Canonical Allele Identifier: PA2828091374
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ala552Thr
CA394268001
NM_001363528.2:c.1654G>A