Allele Registry

Canonical Allele Identifier: PA915984346

Gene: MSH2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

96584

1798942

ClinVar RCV:

RCV000076612

RCV000491974

RCV001249918

RCV001293544

RCV001390798

RCV002340695

RCV003452944

ClinVar Variation:

91109

1744045

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gly98Arg	CA021212 NM_001258281.1:c.292G>A CA346730633 NM_001258281.1:c.292G>C