Canonical Allele Identifier: PA2827020969
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1359198
ClinVar RCV Id: RCV001904352

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.His1690Arg
CA394314615
NM_001318832.2:c.5069A>G