Allele Registry

Canonical Allele Identifier: PA2829977299

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000190005

RCV000644168

RCV002426918

ClinVar Variation:

207734

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Ile893Thr	CA319484 NM_021055.3:c.2678T>C