Canonical Allele Identifier: PA2829201742
Gene: IL18RAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2280170
ClinVar RCV Id: RCV004133739

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380417.1:p.Asn406Asp
CA1810667
NM_001393488.1:c.1216A>G