Canonical Allele Identifier: PA2573095193
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1308444
ClinVar RCV Id: RCV001763356

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Asp291Gly
CA8051415
NM_022162.3:c.872A>G