Canonical Allele Identifier: PA2826182065
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 436987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Leu488Phe
CA3184839
NM_001193376.3:c.1462C>T