Allele Registry

Canonical Allele Identifier: PA2826464357

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000774569

RCV000986673

RCV001201365

ClinVar Variation:

216343

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ser450Asn	CA338107 NM_001258281.1:c.1349G>A