Canonical Allele Identifier: PA2826181955
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 471819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Ala436Val
CA112957696
NM_001193376.3:c.1307C>T