Canonical Allele Identifier: PA1139745759
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_071445.1:p.Thr218Ile
CA395867279
NM_022162.3:c.653C>T