Canonical Allele Identifier: PA096388
Gene: TNFRSF1A HGNC NCBI

Linked Data

ClinVar Variation Id: 12342
ClinVar RCV Id: RCV000013135
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001056.1:p.Cys59Ser
CA280159
NM_001065.4:c.176G>C
CA383550867
NM_001065.4:c.175T>A