Canonical Allele Identifier: PA2829983516
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2416226

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Tyr1693Cys
CA394314314
NM_021055.3:c.5078A>G