Canonical Allele Identifier: PA2499288919
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1035561

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Val487Ile
CA281262812
NM_022162.3:c.1459G>A