Canonical Allele Identifier: PA2828432774
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4701
ClinVar RCV Id: RCV000004966 RCV002512788
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Glu356Lys
CA117031
NM_001370466.1:c.1066G>A