Allele Registry

Canonical Allele Identifier: PA916023474

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000055502

RCV000760985

ClinVar Variation:

65281

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Leu459Pro	CA014458 NM_001318832.2:c.1376T>C