Canonical Allele Identifier: PA129992
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 39121
ClinVar RCV Id: RCV000030632 RCV000032393 RCV000151992 RCV000305704 RCV000395635 RCV001262530 RCV001573195 RCV002513302 RCV002321495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937983.2:p.Ala1062Thr
CA129990
NM_198253.3:c.3184G>A