Canonical Allele Identifier: PA2825437631
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 184243

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Glu1135Lys
CA019256
NM_001077183.3:c.3403G>A