Allele Registry

Canonical Allele Identifier: PA2827020716

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000042603

ClinVar Variation:

49343

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Ser1628Pro	CA021580 NM_001318832.2:c.4882T>C