Allele Registry

Canonical Allele Identifier: PA261390

Gene: MYL2 HGNC NCBI

ClinVar RCV:

RCV000036408

RCV003486556

ClinVar Variation:

43479

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Gly162Glu	CA010439 NM_000432.4:c.485G>A