Allele Registry

Canonical Allele Identifier: PA180713

Gene: MYH7 HGNC NCBI

ClinVar Allele:

175619

ClinVar RCV:

RCV000168873

RCV000622211

RCV000758036

RCV001194066

RCV001798497

ClinVar Variation:

177757

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Lys847Glu	CA012578 NM_000257.4:c.2539A>G