Allele Registry

Canonical Allele Identifier: PA2826465968

Gene: MSH2 HGNC NCBI

ClinVar Allele:

212210

ClinVar RCV:

RCV000198941

RCV000223226

RCV000235290

RCV000412048

RCV003997023

ClinVar Variation:

216359

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Lys843Ile	CA037340 NM_001258281.1:c.2528A>T