Canonical Allele Identifier: PA2828432668
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 936769

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Cys220Phe
CA8051387
NM_001370466.1:c.659G>T