Canonical Allele Identifier: PA2826182607
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 1789927
ClinVar Variation Id: 2936748
ClinVar RCV Id: RCV003798986

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Glu782Asp
CA3184562
NM_001193376.3:c.2346G>T
CA359076304
NM_001193376.3:c.2346G>C