Allele Registry

Canonical Allele Identifier: PA2826465242

Gene: MSH2 HGNC NCBI

ClinVar Allele:

2128543

ClinVar RCV:

RCV002953513

ClinVar Variation:

2064560

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gly655Arg	CA346729346 NM_001258281.1:c.1963G>A CA346729347 NM_001258281.1:c.1963G>C