Allele Registry

Canonical Allele Identifier: PA2826463560

Gene: MSH2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000001832

RCV000030257

RCV000034561

RCV000121567

RCV000144615

RCV000157760

RCV001083998

RCV001262750

RCV001353916

ClinVar Variation:

1762

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gly256Asp	CA022645 NM_001258281.1:c.767G>A CA3054204394 NM_001258281.1:c.767_771delinsACTCC