Canonical Allele Identifier: PA280789
Gene: TNFRSF1A HGNC NCBI

Linked Data

ClinVar Variation Id: 97676
ClinVar RCV Id: RCV000083929 RCV000254771
ClinVar Variation Id: 97679
ClinVar RCV Id: RCV000083932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001056.1:p.Phe89Leu
CA280787
NM_001065.4:c.265T>C
CA280796
NM_001065.4:c.267C>A
CA383550545
NM_001065.4:c.267C>G