Allele Registry

Canonical Allele Identifier: PA277661

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000201453

RCV000456307

RCV001181802

RCV001762425

RCV002345719

RCV002485326

RCV003323452

ClinVar Variation:

217468

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Gly1808Ser	CA046762 NM_000257.4:c.5422G>A