Canonical Allele Identifier: PA2826835890
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4692
ClinVar RCV Id: RCV000268347 RCV000238745 RCV000416490 RCV000996266 RCV001781185 RCV002054415 RCV002260961 RCV002512782
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Gly881Arg
CA117015
NM_001293557.2:c.2641G>C