Allele Registry

Canonical Allele Identifier: PA2828420561

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV001070860

RCV004000195

ClinVar Variation:

863806

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357334.1:p.Pro1401Ser	CA394301401 NM_001370405.1:c.4201C>T