Allele Registry

Canonical Allele Identifier: PA132629

Gene: MYL2 HGNC NCBI

ClinVar RCV:

RCV000030324

RCV000036398

RCV000228967

RCV000618181

RCV000994981

RCV001185060

RCV002482922

RCV003996131

ClinVar Variation:

36645

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Arg120Gln	CA010211 NM_000432.4:c.359G>A