Canonical Allele Identifier: PA2827015723
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1000977
ClinVar RCV Id: RCV001297190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Val1306Phe
CA394305002
NM_001318831.2:c.3916G>T