Canonical Allele Identifier: PA2828432613
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319427
ClinVar RCV Id: RCV000295019 RCV001782791 RCV002227151 RCV002261055 RCV002522853
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Val135Ile
CA8051288
NM_001370466.1:c.403G>A