Allele Registry

Canonical Allele Identifier: PA2829981404

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 238051

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Glu1447Gly	CA051259 NM_021055.3:c.4340A>G