Canonical Allele Identifier: PA1139766069
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 950507

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937983.2:p.Arg691Ser
CA112949480
NM_198253.3:c.2071C>A