Canonical Allele Identifier: PA202827
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 197333
ClinVar RCV Id: RCV000178334 RCV000488013 RCV000368536 RCV001781536 RCV002262774 RCV002517729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Arg703Cys
CA202825
NM_022162.3:c.2107C>T