Canonical Allele Identifier: PA2580450725
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1908341
ClinVar RCV Id: RCV002584128
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Pro80Thr
CA8051229
NM_022162.3:c.238C>A