Canonical Allele Identifier: PA2827009280
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Pro1266Leu
CA020000
NM_001318829.2:c.3797C>T