Canonical Allele Identifier: PA2825573915
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 186281

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Arg628His
CA016151
NM_001114382.3:c.1883G>A