Canonical Allele Identifier: PA2826835236
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1715769
ClinVar RCV Id: RCV002304625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Thr70Ala
CA395866050
NM_001293557.2:c.208A>G