Allele Registry

Canonical Allele Identifier: PA094901

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000076380

RCV000490901

RCV000491588

RCV000821619

RCV001378609

ClinVar Variation:

90878

428477

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gly692Arg	CA019963 NM_000251.3:c.2074G>C CA346729188 NM_000251.3:c.2074G>A