Canonical Allele Identifier: PA2826835265
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1001128
ClinVar RCV Id: RCV002541842

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Ser100Leu
CA8051266
NM_001293557.2:c.299C>T