Canonical Allele Identifier: PA2825438844
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Leu1481Pro
CA020803
NM_001077183.3:c.4442T>C