Canonical Allele Identifier: PA2826835271
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97877
ClinVar RCV Id: RCV000383429 RCV001781430 RCV002513888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Arg111Gln
CA150333
NM_001293557.2:c.332G>A