Allele Registry

Canonical Allele Identifier: PA2829976835

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 467948

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Ala837Gly	CA039285 NM_021055.3:c.2510C>G