Canonical Allele Identifier: PA2825575688
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468020

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Pro1176Ser
CA394289363
NM_001114382.3:c.3526C>T