Canonical Allele Identifier: PA2829201732
Gene: IL18RAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2353191
ClinVar RCV Id: RCV004192542

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380417.1:p.Glu116Gly
CA1810446
NM_001393488.1:c.347A>G