Canonical Allele Identifier: PA645426921
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 306163

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg292Trp
CA6197289
NM_000260.4:c.874C>T