Canonical Allele Identifier: PA2827014314
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65283

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Leu822Pro
CA018667
NM_001318831.2:c.2465T>C