Canonical Allele Identifier: PA2826835606
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1124621
ClinVar RCV Id: RCV002557560

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Arg514Gln
CA8051595
NM_001293557.2:c.1541G>A