Canonical Allele Identifier: PA2828432747
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 462694
ClinVar RCV Id: RCV001811042 RCV002263765 RCV002527760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.His325Arg
CA8051452
NM_001370466.1:c.974A>G