Canonical Allele Identifier: PA2826182506
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 39111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Thr726Met
CA343442
NM_001193376.3:c.2177C>T