Allele Registry

Canonical Allele Identifier: PA2826465504

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000553342

RCV000679305

RCV002456044

RCV004003745

ClinVar Variation:

455560

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Asn726Lys	CA346730082 NM_001258281.1:c.2178T>A CA346730085 NM_001258281.1:c.2178T>G