Canonical Allele Identifier: PA891850786
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 570145
ClinVar RCV Id: RCV002544896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Arg587His
CA8051619
NM_022162.3:c.1760G>A