Allele Registry

Canonical Allele Identifier: PA2826464436

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000076204

RCV000410514

RCV000491263

RCV000524349

RCV000588411

RCV001175346

ClinVar Variation:

90707

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Arg468Cys	CA018706 NM_001258281.1:c.1402C>T