Canonical Allele Identifier: PA916028757
Gene: TNFRSF1A HGNC NCBI

Linked Data

ClinVar Variation Id: 97696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333020.1:p.Val16Met
CA280843
NM_001346091.2:c.46G>A