Allele Registry

Canonical Allele Identifier: PA2829984024

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 207763

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Glu1740Lys	CA055186 NM_021055.3:c.5218G>A