Canonical Allele Identifier: PA2826182092
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 1718202
ClinVar RCV Id: RCV003097935
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Leu505Arg
CA359085226
NM_001193376.3:c.1514T>G