Canonical Allele Identifier: PA2826182086
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 410670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Lys502Arg
CA16611726
NM_001193376.3:c.1505A>G