Canonical Allele Identifier: PA2825439583
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65296
ClinVar RCV Id: RCV000055518

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Leu1683Pro
CA022298
NM_001077183.3:c.5048T>C