Allele Registry

Canonical Allele Identifier: PA2825577453

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 468141

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107854.1:p.Val1688Leu	CA394312457 NM_001114382.3:c.5062G>C CA394312460 NM_001114382.3:c.5062G>T