Canonical Allele Identifier: PA2826182590
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 2942166
ClinVar RCV Id: RCV003805380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Pro771Ala
CA359076434
NM_001193376.3:c.2311C>G