Canonical Allele Identifier: PA2826182316
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 29899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Arg631Gln
CA128724
NM_001193376.3:c.1892G>A