Allele Registry

Canonical Allele Identifier: PA915984280

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000527224

RCV000562713

RCV000781569

RCV001284653

ClinVar Variation:

455593

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Val89Gly	CA346730532 NM_001258281.1:c.266T>G