Canonical Allele Identifier: PA100999
Gene: IL17RD HGNC NCBI

Linked Data

ClinVar Variation Id: 50867
ClinVar RCV Id: RCV000043609 RCV000156943 RCV000442073 RCV001818215
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060033.3:p.Lys131Thr
CA143828
NM_017563.5:c.392A>C