Allele Registry

Canonical Allele Identifier: PA645414859

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000472981

RCV000788584

RCV002051852

ClinVar Variation:

407200

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Asp394Glu	CA16614497 NM_000257.4:c.1182C>A CA389051171 NM_000257.4:c.1182C>G