Canonical Allele Identifier: PA2826181567
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 410690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Ala257Ser
CA16611733
NM_001193376.3:c.769G>T