Allele Registry

Canonical Allele Identifier: PA237397

Gene: MYL2 HGNC NCBI

ClinVar RCV:

RCV000172053

RCV001063811

RCV001180082

RCV002484988

RCV003352788

RCV003998376

ClinVar Variation:

181434

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Arg120Gly	CA010193 NM_000432.4:c.358C>G