Allele Registry

Canonical Allele Identifier: PA094603

Gene: MSH2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000034558

RCV000076617

RCV000115534

RCV000202071

RCV000664313

RCV001083980

RCV001262884

RCV001356983

RCV003149608

RCV004534721

ClinVar Variation:

41650

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ala2Thr	CA021232 NM_000251.3:c.4G>A