Canonical Allele Identifier: PA915997493
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 39121

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Ala999Thr
CA129990
NM_001193376.3:c.2995G>A