Allele Registry

Canonical Allele Identifier: PA658827661

Gene: MYO7A HGNC NCBI

ClinVar Variation Id: 551019

HGVS (amino-acid)	Matching Registered Transcripts
NP_000251.3:p.Arg206Cys	CA6197203 NM_000260.4:c.616C>T