Allele Registry

Canonical Allele Identifier: PA916023058

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000190077

RCV000644198

RCV002453704

ClinVar Variation:

207784

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305760.1:p.Leu898Pro	CA319595 NM_001318831.2:c.2693T>C