Canonical Allele Identifier: PA2826182089
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 566675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Ser504Trp
CA359085244
NM_001193376.3:c.1511C>G