Allele Registry

Canonical Allele Identifier: PA2827003656

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000042789

RCV000254034

RCV001069687

ClinVar Variation:

49529

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305756.1:p.Trp1128Gly	CA019409 NM_001318827.2:c.3382T>G