Canonical Allele Identifier: PA2829977750
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535970

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Glu942Gly
CA276742132
NM_021055.3:c.2825A>G