Canonical Allele Identifier: PA1139679887
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 939527

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg654His
CA6197655
NM_001127180.2:c.1961G>A