Allele Registry

Canonical Allele Identifier: PA105817

Gene: MYH6 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000015214

RCV000037468

RCV000172563

RCV000190123

RCV000201499

RCV000244450

RCV000623034

RCV000656144

RCV000723680

RCV000770446

RCV000852696

ClinVar Variation:

14151

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_002462.2:p.Ala1004Ser	CA134311 NM_002471.4:c.3010G>T