Canonical Allele Identifier: PA2829978792
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1474765
ClinVar RCV Id: RCV002573414

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.His120Arg
CA281250284
NM_022162.3:c.359A>G