Allele Registry

Canonical Allele Identifier: PA2826463413

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000131790

RCV000588299

RCV000688511

RCV000855651

RCV003467187

RCV003998117

ClinVar Variation:

142587

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gly221Ala	CA022444 NM_001258281.1:c.662G>C