Canonical Allele Identifier: PA2828413537
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 184243

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Glu1135Lys
CA019256
NM_001370404.1:c.3403G>A