Allele Registry

Canonical Allele Identifier: PA2827000323

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 486635

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305756.1:p.Trp130Arg	CA394309129 NM_001318827.2:c.388T>A CA394309132 NM_001318827.2:c.388T>C