Canonical Allele Identifier: PA2825577603
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1359198
ClinVar RCV Id: RCV001904352

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.His1723Arg
CA394314615
NM_001114382.3:c.5168A>G