Canonical Allele Identifier: PA2741976039
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2938328
ClinVar RCV Id: RCV003797150

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Ser178Leu
CA2740093319
NM_022162.3:c.533_534delinsTG