Allele Registry

Canonical Allele Identifier: PA2579923507

Gene: MSH2 HGNC NCBI

MaveDb:

Score -5.3708534591

ClinVar RCV:

RCV004522954

ClinVar Variation:

3230840

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gln879Glu	CA346731314 NM_000251.3:c.2635C>G