Canonical Allele Identifier: PA2827010583
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1478025

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ala1667Thr
CA394315690
NM_001318829.2:c.4999G>A