Allele Registry

Canonical Allele Identifier: PA2828433213

Gene: NOD2 HGNC NCBI

ClinVar RCV:

RCV000238745

RCV000268347

RCV000416490

RCV000996266

RCV001781185

RCV002054415

RCV002260961

RCV002512782

ClinVar Variation:

4692

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357395.1:p.Gly881Arg	CA117015 NM_001370466.1:c.2641G>C