Allele Registry

Canonical Allele Identifier: PA180598

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000015190

RCV000154254

RCV001618214

ClinVar Variation:

14129

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Arg453Ser	CA010621 NM_000257.4:c.1357C>A