Canonical Allele Identifier: PA2828094685
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535895

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ala1494Thr
CA052272
NM_001363528.2:c.4480G>A