Canonical Allele Identifier: PA2825577759
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1440541
ClinVar RCV Id: RCV001978883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Pro1758Thr
CA394315676
NM_001114382.3:c.5272C>A