Canonical Allele Identifier: PA645494170
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 267320
ClinVar RCV Id: RCV000258045 RCV002519022
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Leu81Val
CA8051231
NM_022162.3:c.241C>G