Allele Registry

Canonical Allele Identifier: PA094946

Gene: MSH2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

96572

ClinVar RCV:

RCV000115532

RCV000148628

RCV000212585

RCV000588226

RCV000662480

RCV000764421

RCV001085983

RCV001262752

RCV001358588

RCV001798267

RCV004528278

ClinVar Variation:

91097

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ile145Met	CA021158 NM_000251.3:c.435T>G