Canonical Allele Identifier: PA108812
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 29901
ClinVar RCV Id: RCV000022785 RCV000032388 RCV002426516 RCV003764630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937983.2:p.Arg901Trp
CA128729
NM_198253.3:c.2701C>T