Canonical Allele Identifier: PA108858
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 12735
ClinVar RCV Id: RCV000013572 RCV000032389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937983.2:p.Lys902Asn
CA122663
NM_198253.3:c.2706G>C
CA359072147
NM_198253.3:c.2706G>T