Allele Registry

Canonical Allele Identifier: PA131894

Gene: MYH7 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000035831

RCV000171841

RCV000229046

RCV000277164

RCV000282513

RCV000332160

RCV000415867

RCV000618924

RCV000625843

RCV000771360

RCV003320057

ClinVar Variation:

42938

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Val964Leu	CA013168 NM_000257.4:c.2890G>C CA389046688 NM_000257.4:c.2890G>T