Allele Registry

Canonical Allele Identifier: PA916023607

Gene: TSC2 HGNC NCBI

ClinVar Allele:

466089

ClinVar RCV:

RCV000545413

RCV001012884

ClinVar Variation:

467892

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Thr588Ile	CA033165 NM_001318832.2:c.1763C>T