Canonical Allele Identifier: PA2828432732
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4694
ClinVar RCV Id: RCV000004958 RCV000482720 RCV002512784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Arg307Gln
CA117018
NM_001370466.1:c.920G>A