Canonical Allele Identifier: PA2828094365
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Glu1410Lys
CA051101
NM_001363528.2:c.4228G>A