Canonical Allele Identifier: PA2825437044
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 229369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Gly957Glu
CA043736
NM_001077183.3:c.2870G>A