Allele Registry

Canonical Allele Identifier: PA645471231

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000229561

RCV000235910

RCV000491448

RCV003150133

RCV003998761

ClinVar Variation:

237389

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Val78Ile	CA035416 NM_000251.3:c.232G>A