Canonical Allele Identifier: PA2825437604
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535949

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ser1126Leu
CA394289260
NM_001077183.3:c.3377C>T