Canonical Allele Identifier: PA2499288913
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1037619
ClinVar RCV Id: RCV002546914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Ala428Thr
CA395868595
NM_022162.3:c.1282G>A