Allele Registry

Canonical Allele Identifier: PA299397

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000160638

RCV000212589

RCV000556928

RCV001356798

ClinVar Variation:

182598

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ile194Thr	CA021473 NM_000251.3:c.581T>C