Canonical Allele Identifier: PA110522
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4701
ClinVar RCV Id: RCV000004966 RCV002512788
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Glu383Lys
CA117031
NM_022162.3:c.1147G>A