Canonical Allele Identifier: PA2826835216
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1908341
ClinVar RCV Id: RCV002584128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Pro53Thr
CA8051229
NM_001293557.2:c.157C>A