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Query ClinGen evidence for gene-disease validity, dosage, actionability, and variant pathogenicity.
Copy the install command and let the AI configure it · recommended for beginners
No copy-paste install info for "clingen-link" yet — see the docs or source repo.
Use clingen-link to query ClinGen evidence for BRCA1 and breast cancer, then summarize the current validity classification, evidence sources, and key conclusions.
Returns the ClinGen validity classification, an evidence summary, and key citable findings for the gene-disease pair.
Use clingen-link to retrieve dosage sensitivity information for PMP22, including haploinsufficiency or triplosensitivity evidence and classifications.
Outputs the dosage sensitivity assessment with evidence types, classification results, and a brief interpretation.
Use clingen-link to look up ClinGen pathogenicity-related information for a gene variant and whether the gene has an actionability assessment.
Returns a summary of variant pathogenicity-related evidence and the gene's clinical actionability status with key points.
Query gene-disease validity data and detect consensus or conflicts across assertions.
Search clinical evidence, regulatory data, and literature with grounded context.
Query MGI mouse genetics data for markers, mutations, phenotypes, and disease models.
Check drug interactions, dose ranges, and allergy cross-reactivity safely.
Manage virtual clinic records and search medical literature and knowledge bases.
Query missense tolerance, domain annotations, and constrained regions in human transcripts.