Canonical Allele Identifier: PA208778
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 212400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937983.2:p.Val664Leu
CA208776
NM_198253.3:c.1990G>C
CA359080764
NM_198253.3:c.1990G>T