Canonical Allele Identifier: PA2829974588
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 186281

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Arg628His
CA016151
NM_021055.3:c.1883G>A