Canonical Allele Identifier: PA108886
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_937983.2:p.Pro721Arg
CA343440
NM_198253.3:c.2162C>G