Canonical Allele Identifier: PA2826181601
Gene: TERT HGNC NCBI

Linked Data

ClinVar Variation Id: 2048004
ClinVar RCV Id: RCV002918470
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180305.1:p.Val272Ala
CA112915011
NM_001193376.3:c.815T>C