Canonical Allele Identifier: PA2825576481
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ser1426Phe
CA050898
NM_001114382.3:c.4277C>T