Canonical Allele Identifier: PA645418604
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 410690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937983.2:p.Ala257Ser
CA16611733
NM_198253.3:c.769G>T