Canonical Allele Identifier: PA2828432787
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 853895
ClinVar RCV Id: RCV002554411
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Arg366Cys
CA8051484
NM_001370466.1:c.1096C>T