Canonical Allele Identifier: PA2828094898
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Thr1557Ile
CA021153
NM_001363528.2:c.4670C>T