Canonical Allele Identifier: PA2826182600
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 2679141
ClinVar RCV Id: RCV003474056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Val777Leu
CA359076365
NM_001193376.3:c.2329G>T
CA359076366
NM_001193376.3:c.2329G>C