Canonical Allele Identifier: PA2826182981
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 39122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Thr1047Met
CA343457
NM_001193376.3:c.3140C>T