Canonical Allele Identifier: PA2829201708
Gene: IL18RAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2547310
ClinVar RCV Id: RCV004321343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380416.1:p.Asp255Val
CA347938958
NM_001393487.1:c.764A>T