Canonical Allele Identifier: PA2828432701
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1308444
ClinVar RCV Id: RCV001763356

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Asp264Gly
CA8051415
NM_001370466.1:c.791A>G