Canonical Allele Identifier: PA2828415522
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2416226

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Tyr1692Cys
CA394314314
NM_001370404.1:c.5075A>G