Allele Registry

Canonical Allele Identifier: PA2825576467

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV001070860

RCV004000195

ClinVar Variation:

863806

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107854.1:p.Pro1421Ser	CA394301401 NM_001114382.3:c.4261C>T