Allele Registry

Canonical Allele Identifier: PA2829974338

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 535861

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Ser608Thr	CA033723 NM_021055.3:c.1823G>C