Canonical Allele Identifier: PA185868
Gene: IL17RD HGNC NCBI

Linked Data

ClinVar Variation Id: 180145

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060033.3:p.Pro191Leu
CA185867
NM_017563.5:c.572C>T