Canonical Allele Identifier: PA645494176
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319427
ClinVar RCV Id: RCV000295019 RCV001782791 RCV002227151 RCV002261055 RCV002522853
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Val162Ile
CA8051288
NM_022162.3:c.484G>A