ProtVar Map Variant

Map a human protein variant to genomic coordinates and get pathogenicity predictions (AlphaMissense, EVE, ESM, conservation). Accepts three input formats: (1) protein 'ACCESSION CHANGE' e.g. 'P04637 R175H'; (2) dbSNP rsID e.g. 'rs1799966'; (3) VCF-style genomic 'chr17 43057065 . T G'. Returns isoform mappings, consequence type, and variant effect scores.