Allele Registry

Canonical Allele Identifier: PA658672396

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000574584

RCV001223400

RCV003760966

RCV004001117

ClinVar Variation:

485829

2819272

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Met460Ile	CA028148 NM_000251.3:c.1380G>A CA346724829 NM_000251.3:c.1380G>C CA346724830 NM_000251.3:c.1380G>T