Allele Registry

Canonical Allele Identifier: PA2827010749

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 486635

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305758.1:p.Trp118Arg	CA394309129 NM_001318829.2:c.352T>A CA394309132 NM_001318829.2:c.352T>C