Allele Registry

Canonical Allele Identifier: PA2829980274

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 486606

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Ser1303Leu	CA050248 NM_021055.3:c.3908C>T