Allele Registry

Canonical Allele Identifier: PA2826463734

Gene: MSH2 HGNC NCBI

ClinVar Allele:

152481

ClinVar RCV:

RCV000132158

RCV000225952

RCV001192615

RCV001249911

RCV003453092

RCV003477557

ClinVar Variation:

142767

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Arg293Thr	CA017103 NM_001258281.1:c.878G>C