Canonical Allele Identifier: PA2827016421
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2416226

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Tyr1492Cys
CA394314314
NM_001318831.2:c.4475A>G