Canonical Allele Identifier: PA2580450938
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2003783
ClinVar RCV Id: RCV002811436

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Glu748Asp
CA281264176
NM_022162.3:c.2244G>C
CA395871503
NM_022162.3:c.2244G>T