Canonical Allele Identifier: PA645494171
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319425
ClinVar RCV Id: RCV000268742 RCV001782789 RCV001812837 RCV002521016 RCV002521017 RCV002261053
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Val92Ile
CA8051239
NM_022162.3:c.274G>A