Canonical Allele Identifier: PA2826182060
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 39101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Arg486Cys
CA343424
NM_001193376.3:c.1456C>T