Allele Registry

Canonical Allele Identifier: PA658802971

Gene: MYL2 HGNC NCBI

ClinVar RCV:

RCV000639677

RCV001575874

ClinVar Variation:

532778

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Arg58Leu	CA386698863 NM_000432.4:c.173G>T