Canonical Allele Identifier: PA2828432905
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 646734

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Thr484Ala
CA8051565
NM_001370466.1:c.1450A>G