Canonical Allele Identifier: PA108876
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 39108
ClinVar RCV Id: RCV000022786 RCV000032375 RCV000520116 RCV002509175 RCV003103717 RCV002415443 RCV003460537
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937983.2:p.Pro704Ser
CA128731
NM_198253.3:c.2110C>T