Canonical Allele Identifier: PA2580297756
Gene: IL18RAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2280170
ClinVar RCV Id: RCV004133739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003844.1:p.Asn548Asp
CA1810667
NM_003853.3:c.1642A>G