Allele Registry

Canonical Allele Identifier: PA915981262

Gene: MYO7A HGNC NCBI

ClinVar RCV:

RCV000416022

ClinVar Variation:

374511

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120652.1:p.Cys1201Tyr	CA16043772 NM_001127180.2:c.3602G>A