ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826835890
Gene: NOD2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000238745
RCV000268347
RCV000416490
RCV000996266
RCV001781185
RCV002054415
RCV002260961
RCV002512782
ClinVar Variation:
4692
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001280486.1:p.Gly881Arg
CA117015
NM_001293557.2:c.2641G>C