Allele Registry

Canonical Allele Identifier: PA2826462947

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000697263

RCV001184535

RCV001731362

RCV001800375

RCV003452948

ClinVar Variation:

91125

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Leu109Pro	CA021302 NM_001258281.1:c.326T>C