Canonical Allele Identifier: PA2828432667
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319434
ClinVar RCV Id: RCV000274697 RCV001782798 RCV002522855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Thr218Met
CA8051383
NM_001370466.1:c.653C>T