Allele Registry

Canonical Allele Identifier: PA099079

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV001054191

RCV002285271

ClinVar Variation:

181338

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Val404Met	CA010379 NM_000257.4:c.1210G>A