Canonical Allele Identifier: PA2825577554
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 951296

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Thr1710Pro
CA394314222
NM_001114382.3:c.5128A>C