Canonical Allele Identifier: PA2826181858
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 1735586
ClinVar RCV Id: RCV002366228
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Tyr386Cys
CA359086709
NM_001193376.3:c.1157A>G