Allele Registry

Canonical Allele Identifier: PA916023972

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000055281

RCV001853092

ClinVar Variation:

65074

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Ala900Pro	CA017834 NM_001318832.2:c.2698G>C