Canonical Allele Identifier: PA2826835729
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319460
ClinVar RCV Id: RCV000372158 RCV001782822 RCV002261062 RCV002522866
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Arg689His
CA8051707
NM_001293557.2:c.2066G>A