Canonical Allele Identifier: PA117017
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4692
ClinVar RCV Id: RCV000268347 RCV000238745 RCV000416490 RCV000996266 RCV001781185 RCV002054415 RCV002260961 RCV002512782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Gly908Arg
CA117015
NM_022162.3:c.2722G>C