Canonical Allele Identifier: PA2826835584
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 449632
ClinVar RCV Id: RCV000520892 RCV002261098 RCV002525125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Tyr487His
CA8051566
NM_001293557.2:c.1459T>C