Canonical Allele Identifier: PA2828421680
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1359198
ClinVar RCV Id: RCV001904352

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.His1699Arg
CA394314615
NM_001370405.1:c.5096A>G