Allele Registry

Canonical Allele Identifier: PA2826465113

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000076380

RCV000490901

RCV000491588

RCV000821619

RCV001378609

ClinVar Variation:

90878

428477

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gly626Arg	CA019963 NM_001258281.1:c.1876G>C CA346729188 NM_001258281.1:c.1876G>A