Allele Registry

Canonical Allele Identifier: PA177009

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000151251

RCV000766443

ClinVar Variation:

164305

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Arg1079Gly	CA013459 NM_000257.4:c.3235C>G