Canonical Allele Identifier: PA2829201722
Gene: IL18RAP HGNC NCBI

Linked Data

ClinVar Variation Id: 3109206
ClinVar RCV Id: RCV004405073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380416.1:p.Thr575Ile
CA1810679
NM_001393487.1:c.1724C>T