Canonical Allele Identifier: PA2826182085
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 2102176
ClinVar RCV Id: RCV003019397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Lys502Asn
CA359085267
NM_001193376.3:c.1506G>T
CA359085270
NM_001193376.3:c.1506G>C