Allele Registry

Canonical Allele Identifier: PA296922

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000158882

RCV000536809

RCV000584771

RCV001187174

RCV001270160

ClinVar Variation:

181402

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Asp309Asn	CA016961 NM_000257.4:c.925G>A