Canonical Allele Identifier: PA108951
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 242228

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937983.2:p.Val791Ile
CA044696
NM_198253.3:c.2371G>A