Canonical Allele Identifier: PA174385
Gene: TNFRSF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 161578
ClinVar RCV Id: RCV000149113
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001234.3:p.Asp91Tyr
CA174384
NM_001243.5:c.271G>T