Canonical Allele Identifier: PA2826835373
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319439

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.His260Tyr
CA8051412
NM_001293557.2:c.778C>T