Allele Registry

Canonical Allele Identifier: PA645475457

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000491379

RCV001215708

RCV003449383

ClinVar Variation:

428567

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Val702Glu	CA346729242 NM_000251.3:c.2105T>A