Allele Registry

Canonical Allele Identifier: PA338305

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000198941

RCV000223226

RCV000235290

RCV000412048

RCV003997023

ClinVar Variation:

216359

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Lys909Ile	CA037340 NM_000251.3:c.2726A>T