Canonical Allele Identifier: PA2828092684
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_001350457.1:p.Thr913Pro
CA394279610
NM_001363528.2:c.2737A>C