Allele Registry

Canonical Allele Identifier: PA915984309

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000160612

RCV000212587

RCV000477198

RCV001002118

RCV003444208

ClinVar Variation:

182580

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Val95Ile	CA021193 NM_001258281.1:c.283G>A