Canonical Allele Identifier: PA2826835462
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2160470
ClinVar RCV Id: RCV003075969

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Glu365Lys
CA8051483
NM_001293557.2:c.1093G>A