Allele Registry

Canonical Allele Identifier: PA645434729

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 238051

HGVS (amino-acid)	Matching Registered Transcripts
NP_000539.2:p.Glu1490Gly	CA051259 NM_000548.5:c.4469A>G