Canonical Allele Identifier: PA2825574925
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1795355
ClinVar RCV Id: RCV002437540 RCV003512186
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Thr913Pro
CA394279610
NM_001114382.3:c.2737A>C