Allele Registry

Canonical Allele Identifier: PA153817

Gene: MYH8 HGNC NCBI

ClinVar RCV:

RCV000117685

RCV000354138

RCV001689650

ClinVar Variation:

129671

HGVS (amino-acid)	Matching Registered Transcripts
NP_002463.2:p.Ala636Val	CA153816 NM_002472.3:c.1907C>T