Allele Registry

Canonical Allele Identifier: PA2827019834

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV001070860

RCV004000195

ClinVar Variation:

863806

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Pro1388Ser	CA394301401 NM_001318832.2:c.4162C>T