Allele Registry

Canonical Allele Identifier: PA2827002800

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000055281

RCV001853092

ClinVar Variation:

65074

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305756.1:p.Ala852Pro	CA017834 NM_001318827.2:c.2554G>C