Canonical Allele Identifier: PA916057886
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 665298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937983.2:p.Ala518Ser
CA3184828
NM_198253.3:c.1552G>T