Canonical Allele Identifier: PA2827019628
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Pro1325Leu
CA020000
NM_001318832.2:c.3974C>T