Canonical Allele Identifier: PA2828095347
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2416226

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Tyr1670Cys
CA394314314
NM_001363528.2:c.5009A>G