Canonical Allele Identifier: PA2826835328
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 885263
ClinVar RCV Id: RCV001116757 RCV001784651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Thr191Ile
CA395867279
NM_001293557.2:c.572C>T