Allele Registry

Canonical Allele Identifier: PA658804441

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000622746

ClinVar Variation:

520452

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Gly584Cys	CA389049895 NM_000257.4:c.1750G>T