Canonical Allele Identifier: PA150376
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97902
ClinVar RCV Id: RCV000084160 RCV002262685 RCV001753488 RCV002513891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Arg373Cys
CA150374
NM_022162.3:c.1117C>T