Allele Registry

Canonical Allele Identifier: PA331435

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000076363

RCV000254985

RCV002415560

RCV003452882

ClinVar Variation:

90861

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gly674Asp	CA019835 NM_000251.3:c.2021G>A