Canonical Allele Identifier: PA2828094242
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50125

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Glu1376Lys
CA020286
NM_001363528.2:c.4126G>A