Allele Registry

Canonical Allele Identifier: PA645416612

Gene: MYH7 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000290926

RCV000320862

RCV000378340

RCV000379421

RCV000489125

RCV000777729

RCV001364427

RCV001729526

RCV002436162

RCV003320163

ClinVar Variation:

312903

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Ala1012Asp	CA035299 NM_000257.4:c.3035C>A