Allele Registry

Canonical Allele Identifier: PA2825574847

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000055281

RCV001853092

ClinVar Variation:

65074

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107854.1:p.Ala889Pro	CA017834 NM_001114382.3:c.2665G>C