Allele Registry

Canonical Allele Identifier: PA2829980501

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000055577

RCV000475654

RCV003162432

ClinVar Variation:

65353

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Pro1338Leu	CA020000 NM_021055.3:c.4013C>T