Canonical Allele Identifier: PA2826181735
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 2049209
ClinVar RCV Id: RCV002909593

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Pro322Ser
CA359056062
NM_001193376.3:c.964C>T