Canonical Allele Identifier: PA150344
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97881
ClinVar RCV Id: RCV000084138 RCV001811399 RCV002260989 RCV002514490
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Leu248Arg
CA150342
NM_022162.3:c.743T>G