Canonical Allele Identifier: PA2826182022
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 539202
ClinVar Variation Id: 2940965
ClinVar RCV Id: RCV003792227

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Val465Leu
CA3184848
NM_001193376.3:c.1393G>C
CA359085812
NM_001193376.3:c.1393G>T