Canonical Allele Identifier: PA2826835582
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 646734

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Thr484Ala
CA8051565
NM_001293557.2:c.1450A>G