Canonical Allele Identifier: PA280795
Gene: TNFRSF1A HGNC NCBI

Linked Data

ClinVar Variation Id: 97678
ClinVar RCV Id: RCV000083931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001056.1:p.Phe89Ser
CA280793
NM_001065.4:c.266T>C