Canonical Allele Identifier: PA2825571869
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486676

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Glu13Lys
CA394300845
NM_001114382.3:c.37G>A