Canonical Allele Identifier: PA2829970363
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 951243

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Leu45Pro
CA394301801
NM_021055.3:c.134T>C