Canonical Allele Identifier: PA2826835554
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2939629
ClinVar RCV Id: RCV003794795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Gly454Ser
CA281262728
NM_001293557.2:c.1360G>A