Canonical Allele Identifier: PA2826182752
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 12736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Arg865His
CA122665
NM_001193376.3:c.2594G>A