Canonical Allele Identifier: PA1139743005
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 952371
ClinVar RCV Id: RCV002562593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Arg992Gly
CA8052067
NM_001370466.1:c.2974C>G