Canonical Allele Identifier: PA2828094646
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1000977
ClinVar RCV Id: RCV001297190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Val1484Phe
CA394305002
NM_001363528.2:c.4450G>T