Canonical Allele Identifier: PA2826182122
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 1711599

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Arg521His
CA359085031
NM_001193376.3:c.1562G>A