Allele Registry

Canonical Allele Identifier: PA916023682

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000424565

RCV001865357

ClinVar Variation:

385710

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Ala634Val	CA16608037 NM_001318832.2:c.1901C>T