Canonical Allele Identifier: PA2826835232
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319425
ClinVar RCV Id: RCV000268742 RCV001782789 RCV001812837 RCV002521016 RCV002521017 RCV002261053
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Val65Ile
CA8051239
NM_001293557.2:c.193G>A