Canonical Allele Identifier: PA2826181931
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 1025387
ClinVar RCV Id: RCV002546136

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Cys426Trp
CA359086382
NM_001193376.3:c.1278T>G