Allele Registry

Canonical Allele Identifier: PA186472

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000162561

RCV000168102

RCV000585899

RCV000663034

RCV000761166

ClinVar Variation:

183783

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Glu569Gly	CA019085 NM_000251.3:c.1706A>G