Canonical Allele Identifier: PA2826835560
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1035561

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Val460Ile
CA281262812
NM_001293557.2:c.1378G>A