Allele Registry

Canonical Allele Identifier: PA2829983985

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000548829

RCV000615984

RCV002350301

ClinVar Variation:

468161

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Thr1737Pro	CA276760048 NM_021055.3:c.5209A>C