Allele Registry

Canonical Allele Identifier: PA2825576464

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV001929846

ClinVar Variation:

1365523

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107854.1:p.Gly1420Ser	CA394301372 NM_001114382.3:c.4258G>A