Allele Registry

Canonical Allele Identifier: PA180957

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000464365

RCV000622007

RCV000770500

RCV000786167

RCV002051819

ClinVar Variation:

177897

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Arg442Cys	CA010561 NM_000257.4:c.1324C>T