Canonical Allele Identifier: PA2828095109
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Glu1613Lys
CA021570
NM_001363528.2:c.4837G>A