berntpopp

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Access multiple gene data backends through one searchable unified MCP endpoint.

Access multiple biomedical MCP data services through one unified endpoint.

Resolve gene symbols and IDs to canonical HGNC records and cross-references.

Query gene-disease validity data and detect consensus or conflicts across assertions.

Query MGI mouse genetics data for markers, mutations, phenotypes, and disease models.

Query ClinGen evidence for gene-disease validity, dosage, actionability, and variant pathogenicity.

Query missense tolerance, domain annotations, and constrained regions in human transcripts.

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