Canonical Allele Identifier: PA2828415559
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1359198
ClinVar RCV Id: RCV001904352

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.His1702Arg
CA394314615
NM_001370404.1:c.5105A>G