Canonical Allele Identifier: PA2826181963
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 212398
ClinVar RCV Id: RCV000192469 RCV000275900 RCV000370254 RCV000312359 RCV001261857 RCV000726693 RCV000768107 RCV001843492 RCV002517983 RCV004530148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Glu441del
CA205307
NM_001193376.3:c.1323_1325del
CA359086208
NM_001193376.3:c.1321G>T
CA359086227
NM_001193376.3:c.1318G>T
CA359086245
NM_001193376.3:c.1315G>T