Canonical Allele Identifier: PA2826835408
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1059021
ClinVar RCV Id: RCV002550075

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Cys306Tyr
CA395868015
NM_001293557.2:c.917G>A