Allele Registry

Canonical Allele Identifier: PA2828415711

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000548829

RCV000615984

RCV002350301

ClinVar Variation:

468161

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357333.1:p.Thr1736Pro	CA276760048 NM_001370404.1:c.5206A>C