Allele Registry

Canonical Allele Identifier: PA2825577513

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV001887213

RCV002334832

ClinVar Variation:

1395605

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107854.1:p.Gln1701Glu	CA394313923 NM_001114382.3:c.5101C>G