Canonical Allele Identifier: PA2827000074
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1915555
ClinVar RCV Id: RCV002601573

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Ala42Thr
CA394301705
NM_001318827.2:c.124G>A