Allele Registry

Canonical Allele Identifier: PA2827004193

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000426687

RCV003626619

ClinVar Variation:

380381

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305756.1:p.Pro1286Ser	CA16607165 NM_001318827.2:c.3856C>T