Allele Registry

Canonical Allele Identifier: PA645415941

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000485371

RCV002526965

ClinVar Variation:

423978

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Ser738Cys	CA16619851 NM_000257.4:c.2212A>T