Allele Registry

Canonical Allele Identifier: PA915980795

Gene: MYO7A HGNC NCBI

ClinVar RCV:

RCV000012638

RCV001723559

ClinVar Variation:

11863

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120652.1:p.Asn458Ile	CA256098 NM_001127180.2:c.1373A>T