Canonical Allele Identifier: PA2828432615
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1969188
ClinVar RCV Id: RCV002755368

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Cys140Gly
CA8051293
NM_001370466.1:c.418T>G