Canonical Allele Identifier: PA2826835412
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4694

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Arg307Gln
CA117018
NM_001293557.2:c.920G>A