Allele Registry

Canonical Allele Identifier: PA915980785

Gene: MYO7A HGNC NCBI

ClinVar RCV:

RCV000036048

RCV002513368

ClinVar Variation:

43144

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120652.1:p.Ala457Val	CA278624 NM_001127180.2:c.1370C>T