Canonical Allele Identifier: PA2829979420
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50148

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Gly1161Glu
CA019384
NM_021055.3:c.3482G>A