Allele Registry

Canonical Allele Identifier: PA2499232334

Gene: MYL2 HGNC NCBI

ClinVar RCV:

RCV001337424

ClinVar Variation:

1034666

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Arg40Thr	CA243563297 NM_000432.4:c.119G>C