Allele Registry

Canonical Allele Identifier: PA279279

Gene: MYL2 HGNC NCBI

ClinVar RCV:

RCV000201445

RCV001178807

RCV002426954

ClinVar Variation:

217490

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Gly42Asp	CA279277 NM_000432.4:c.125G>A