Canonical Allele Identifier: PA658810086
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 539219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937983.2:p.Ala190Val
CA3184954
NM_198253.3:c.569C>T