Canonical Allele Identifier: PA2825179402
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2679345

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ala42Gly
CA394301721
NM_000548.5:c.125C>G