Canonical Allele Identifier: PA2826181902
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 12730
ClinVar RCV Id: RCV000013567 RCV000032365 RCV000190902 RCV000218461 RCV000262966 RCV000425346 RCV002255259 RCV002362581 RCV003224095 RCV002513014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.His412Tyr
CA122655
NM_001193376.3:c.1234C>T