Allele Registry

Canonical Allele Identifier: PA915983983

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000030251

RCV000130254

RCV000236541

RCV000536977

RCV000657039

RCV000662359

RCV004532423

ClinVar Variation:

36575

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Val36Ile	CA020996 NM_001258281.1:c.106G>A