Canonical Allele Identifier: PA2580297751
Gene: IL18RAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2353191
ClinVar RCV Id: RCV004192542

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003844.1:p.Glu258Gly
CA1810446
NM_003853.3:c.773A>G