Canonical Allele Identifier: PA2825439563
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1359198
ClinVar RCV Id: RCV001904352

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.His1679Arg
CA394314615
NM_001077183.3:c.5036A>G