Canonical Allele Identifier: PA2826182499
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 39110
ClinVar RCV Id: RCV000032377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Pro721Arg
CA343440
NM_001193376.3:c.2162C>G