Canonical Allele Identifier: PA2828432670
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97881

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Leu221Arg
CA150342
NM_001370466.1:c.662T>G