Canonical Allele Identifier: PA2827016503
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Glu1512Lys
CA054884
NM_001318831.2:c.4534G>A