Canonical Allele Identifier: PA2827019810
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50124

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Arg1382Gln
CA020250
NM_001318832.2:c.4145G>A