Canonical Allele Identifier: PA2499288916
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1163981

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Arg468Cys
CA8051539
NM_022162.3:c.1402C>T