Canonical Allele Identifier: PA2828432907
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 449632
ClinVar RCV Id: RCV000520892 RCV002261098 RCV002525125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Tyr487His
CA8051566
NM_001370466.1:c.1459T>C