Canonical Allele Identifier: PA2828089709
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2679345

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ala42Gly
CA394301721
NM_001363528.2:c.125C>G