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Resolve gene symbols and IDs to canonical HGNC records and cross-references.
Copy the install command and let the AI configure it · recommended for beginners
No copy-paste install info for "hgnc-link" yet — see the docs or source repo.
Use hgnc-link to look up the gene symbol BRCA1 and return its canonical HGNC ID, approved name, aliases, and common cross-reference database identifiers.
Returns the standard HGNC record for BRCA1, including canonical symbol, name, HGNC ID, and related database cross-references.
Use hgnc-link to batch process these gene symbols: TP53, EGFR, VEGFA, HER2, MTOR. Map any non-canonical names to standard HGNC symbols and output a table with the corresponding HGNC IDs.
Outputs a normalization table showing original input, canonical symbol, HGNC ID, and notes for unmatched or renamed entries.
I have a list of HGNC IDs. Use hgnc-link to add Ensembl, NCBI Gene, and UniProt cross-references for each gene and organize them into an exportable list.
Returns a gene annotation list with external database identifiers for downstream integration, analysis, or import.
Look up HGNC gene nomenclature, symbols, aliases, and related gene information.
Query gene-disease validity data and detect consensus or conflicts across assertions.
Access multiple gene data backends through one searchable unified MCP endpoint.
Query ClinGen evidence for gene-disease validity, dosage, actionability, and variant pathogenicity.
Access NIH, WHO, and genetic variant data for health research and analysis.
Search and download NCBI GEO gene expression data using natural language.