Canonical Allele Identifier: PA2829201690
Gene: IL18RAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2515572
ClinVar RCV Id: RCV004296162
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380415.1:p.Ala496Gly
CA1810647
NM_001393486.1:c.1487C>G