Canonical Allele Identifier: PA1139743002
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 961982
ClinVar RCV Id: RCV002261314 RCV002563837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Arg982Gly
CA8052049
NM_001370466.1:c.2944A>G