Allele Registry

Canonical Allele Identifier: PA2826464177

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000557128

RCV000570076

RCV001798872

RCV003459175

ClinVar Variation:

455487

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Asn399Ser	CA346726685 NM_001258281.1:c.1196A>G