Allele Registry

Canonical Allele Identifier: PA2827005663

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000548829

RCV000615984

RCV002350301

ClinVar Variation:

468161

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305756.1:p.Thr1677Pro	CA276760048 NM_001318827.2:c.5029A>C