Allele Registry

Canonical Allele Identifier: PA132627

Gene: MYL2 HGNC NCBI

ClinVar RCV:

RCV000036397

RCV000770393

RCV001056367

RCV003133123

RCV003996226

ClinVar Variation:

43471

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Arg120Trp	CA010200 NM_000432.4:c.358C>T