Canonical Allele Identifier: PA2828432764
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97902

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Arg346Cys
CA150374
NM_001370466.1:c.1036C>T