Allele Registry

Canonical Allele Identifier: PA2829981512

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 535877

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Ser1464Tyr	CA051496 NM_021055.3:c.4391C>A