Canonical Allele Identifier: PA150264
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97850
ClinVar RCV Id: RCV000366861 RCV001781420 RCV001811396 RCV002513879 RCV002260979
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Arg791Gln
CA150262
NM_022162.3:c.2372G>A