Canonical Allele Identifier: PA2826835279
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1020537
ClinVar RCV Id: RCV002543794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Leu126Arg
CA281250450
NM_001293557.2:c.377T>G