Allele Registry

Canonical Allele Identifier: PA916023612

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 535878

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Ala591Gly	CA033236 NM_001318832.2:c.1772C>G