Allele Registry

Canonical Allele Identifier: PA2827020696

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000190039

RCV001084596

RCV002336507

ClinVar Variation:

207758

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Cys1624Tyr	CA053573 NM_001318832.2:c.4871G>A