Canonical Allele Identifier: PA2573278050
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1410907
ClinVar RCV Id: RCV002557641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Gln135Arg
CA8051271
NM_022162.3:c.404A>G