Canonical Allele Identifier: PA096363
Gene: TNFRSF1A HGNC NCBI

Linked Data

ClinVar Variation Id: 12339
ClinVar RCV Id: RCV000013132
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001056.1:p.Cys117Arg
CA280153
NM_001065.4:c.349T>C