Allele Registry

Canonical Allele Identifier: PA2829974088

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 535878

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Ala580Gly	CA033236 NM_021055.3:c.1739C>G