Allele Registry

Canonical Allele Identifier: PA2829977154

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 486642

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Pro874Leu	CA276741554 NM_021055.3:c.2621C>T