Allele Registry

Canonical Allele Identifier: PA296958

Gene: MYL2 HGNC NCBI

ClinVar RCV:

RCV000158913

RCV000852440

RCV001850228

RCV004019921

ClinVar Variation:

181425

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Phe18Ser	CA010495 NM_000432.4:c.53T>C