Canonical Allele Identifier: PA2828432882
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1035561

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Val460Ile
CA281262812
NM_001370466.1:c.1378G>A