Allele Registry

Canonical Allele Identifier: PA1139676219

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001035991

ClinVar Variation:

835167

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Lys29Glu	CA346728707 NM_000251.3:c.85A>G