Canonical Allele Identifier: PA2828415537
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65333
ClinVar RCV Id: RCV000055557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ala1698_Ile1703del
CA022183
NM_001370404.1:c.5092_5109del