Canonical Allele Identifier: PA2829977494
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_066399.2:p.Thr913Pro
CA394279610
NM_021055.3:c.2737A>C