Allele Registry

Canonical Allele Identifier: PA325798

Gene: MYH7 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

52190

ClinVar RCV:

RCV000035914

RCV000172762

RCV000203136

RCV000254102

RCV000331016

RCV000712360

RCV000758034

RCV000852699

ClinVar Variation:

43020

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Ser1491Cys	CA015008 NM_000257.4:c.4472C>G