Allele Registry

Canonical Allele Identifier: PA915981071

Gene: MYO7A HGNC NCBI

ClinVar Variation Id: 177733

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120652.1:p.Gly955Ser	CA278729 NM_001127180.2:c.2863G>A