Canonical Allele Identifier: PA2825434147
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2679345

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ala42Gly
CA394301721
NM_001077183.3:c.125C>G