Canonical Allele Identifier: PA2825438859
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49310

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Glu1485del
CA020824
NM_001077183.3:c.4454_4456del