Canonical Allele Identifier: PA2829201759
Gene: IL18RAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2319373
ClinVar RCV Id: RCV004168227
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380418.1:p.Phe372Tyr
CA1810652
NM_001393489.1:c.1115T>A