Canonical Allele Identifier: PA645418676
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 410696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937983.2:p.Ser523Arg
CA16611722
NM_198253.3:c.1569C>G
CA359085010
NM_198253.3:c.1569C>A
CA359085018
NM_198253.3:c.1567A>C