Allele Registry

Canonical Allele Identifier: PA658804973

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 535878

HGVS (amino-acid)	Matching Registered Transcripts
NP_000539.2:p.Ala580Gly	CA033236 NM_000548.5:c.1739C>G