Allele Registry

Canonical Allele Identifier: PA915986609

Gene: TSC1 HGNC NCBI

ClinVar RCV:

RCV000220036

RCV001041403

ClinVar Variation:

231802

HGVS (amino-acid)	Matching Registered Transcripts
NP_001155898.1:p.Val96Ala	CA034878 NM_001162426.2:c.287T>C