Canonical Allele Identifier: PA2826835956
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 961982

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Arg982Gly
CA8052049
NM_001293557.2:c.2944A>G