Canonical Allele Identifier: PA645470266
Gene: IL17B HGNC NCBI

Linked Data

ClinVar Variation Id: 225702
ClinVar RCV Id: RCV000491934
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055258.1:p.Cys176Tyr
CA129032405
NM_014443.3:c.527G>A