Canonical Allele Identifier: PA2580450733
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1715769
ClinVar RCV Id: RCV002304625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Thr97Ala
CA395866050
NM_022162.3:c.289A>G