Allele Registry

Canonical Allele Identifier: PA2829976586

Gene: TSC2 HGNC NCBI

ClinVar Allele:

59344

ClinVar RCV:

RCV000043451

RCV000430436

RCV001705694

ClinVar Variation:

50182

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Pro816Leu	CA017430 NM_021055.3:c.2447C>T