Canonical Allele Identifier: PA2826835350
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1923914
ClinVar RCV Id: RCV002609233

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Asp223Asn
CA395867478
NM_001293557.2:c.667G>A