Allele Registry

Canonical Allele Identifier: PA2827001778

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 535880

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305756.1:p.Pro568Leu	CA394272977 NM_001318827.2:c.1703C>T