Canonical Allele Identifier: PA2826181598
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 1024656
ClinVar RCV Id: RCV003103970
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Cys271Ser
CA359056682
NM_001193376.3:c.812G>C
CA359056689
NM_001193376.3:c.811T>A