Allele Registry

Canonical Allele Identifier: PA891846898

Gene: MSH2 HGNC NCBI

MaveDb:

Score -2.658404269

ClinVar RCV:

RCV000693598

RCV003584715

RCV003999599

ClinVar Variation:

572259

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Asn127Thr	CA346730352 NM_000251.3:c.380A>C