Canonical Allele Identifier: PA108775
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 12729
ClinVar RCV Id: RCV000013566 RCV000032398 RCV000489117 RCV000604322 RCV000758251 RCV002255997 RCV002354159 RCV002513013 RCV004541000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937983.2:p.Ala202Thr
CA122653
NM_198253.3:c.604G>A