Canonical Allele Identifier: PA2827012451
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1424794

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Glu283Gln
CA394325437
NM_001318831.2:c.847G>C