Canonical Allele Identifier: PA2829979902
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 648165
ClinVar RCV Id: RCV002261217 RCV002534725
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Ala1000Thr
CA395876750
NM_022162.3:c.2998G>A