Canonical Allele Identifier: PA2825576554
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535938

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Pro1445Leu
CA051050
NM_001114382.3:c.4334C>T