Canonical Allele Identifier: PA2827000043
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 971297

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Glu32Lys
CA394301415
NM_001318827.2:c.94G>A