Allele Registry

Canonical Allele Identifier: PA296950

Gene: MYL2 HGNC NCBI

ClinVar RCV:

RCV000158908

RCV000223748

RCV002515080

ClinVar Variation:

181421

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Glu163Gly	CA010454 NM_000432.4:c.488A>G