Allele Registry

Canonical Allele Identifier: PA2826465581

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000580076

RCV001236705

RCV003061533

RCV003465291

ClinVar Variation:

489937

2151932

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Thr746Ser	CA346730268 NM_001258281.1:c.2236A>T CA346730271 NM_001258281.1:c.2237C>G