Canonical Allele Identifier: PA2825438466
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ser1382Phe
CA050898
NM_001077183.3:c.4145C>T