Allele Registry

Canonical Allele Identifier: PA261386

Gene: MYL2 HGNC NCBI

ClinVar Allele:

52629

ClinVar RCV:

RCV000626688

RCV001588846

RCV002513380

ClinVar Variation:

43459

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Glu65Lys	CA009936 NM_000432.4:c.193G>A