Allele Registry

Canonical Allele Identifier: PA261394

Gene: MYL2 HGNC NCBI

ClinVar RCV:

RCV000036410

RCV000845333

RCV001852758

ClinVar Variation:

43481

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Gln27Arg	CA010526 NM_000432.4:c.80A>G