Canonical Allele Identifier: PA2825435323
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467858

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Tyr429Cys
CA029149
NM_001077183.3:c.1286A>G