Allele Registry

Canonical Allele Identifier: PA2825577754

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000548829

RCV000615984

RCV002350301

ClinVar Variation:

468161

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107854.1:p.Thr1757Pro	CA276760048 NM_001114382.3:c.5269A>C