Allele Registry

Canonical Allele Identifier: PA658802983

Gene: MYL2 HGNC NCBI

ClinVar Allele:

526918

ClinVar RCV:

RCV000639676

ClinVar Variation:

532777

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Thr125Lys	CA386697753 NM_000432.4:c.374C>A