Canonical Allele Identifier: PA2825577330
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Glu1656Lys
CA021570
NM_001114382.3:c.4966G>A