Allele Registry

Canonical Allele Identifier: PA2826465713

Gene: MSH2 HGNC NCBI

ClinVar Allele:

221249

ClinVar RCV:

RCV000204877

RCV000491044

RCV001570632

RCV003997603

ClinVar Variation:

220024

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ala782Ser	CA036472 NM_001258281.1:c.2344G>T