Allele Registry

Canonical Allele Identifier: PA177172

Gene: MYL2 HGNC NCBI

ClinVar RCV:

RCV000151367

RCV000464490

RCV000624062

RCV000766478

RCV001293059

RCV002345474

ClinVar Variation:

164481

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Arg40Lys	CA009847 NM_000432.4:c.119G>A