Canonical Allele Identifier: PA2826181954
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 1718332
ClinVar RCV Id: RCV003097939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Val435Leu
CA359086306
NM_001193376.3:c.1303G>T
CA359086308
NM_001193376.3:c.1303G>C