Canonical Allele Identifier: PA2826181599
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 2200048

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Cys271Gly
CA359056686
NM_001193376.3:c.811T>G