Allele Registry

Canonical Allele Identifier: PA916023745

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 535899

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Gly682Asp	CA035599 NM_001318832.2:c.2045G>A