Allele Registry

Canonical Allele Identifier: PA261392

Gene: MYL2 HGNC NCBI

ClinVar RCV:

RCV000036409

RCV000639678

RCV001193582

ClinVar Variation:

43480

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Glu163Ala	CA010447 NM_000432.4:c.488A>C