Allele Registry

Canonical Allele Identifier: PA645414829

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000490207

RCV001202751

ClinVar Variation:

427102

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Gly377Asp	CA389051291 NM_000257.4:c.1130G>A