Canonical Allele Identifier: PA2828433222
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2929588
ClinVar RCV Id: RCV003784754

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Ala889Thr
CA395875115
NM_001370466.1:c.2665G>A