Canonical Allele Identifier: PA916022793
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Leu82Arg
CA394306574
NM_001318827.2:c.245T>G