Canonical Allele Identifier: PA2827016438
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65333
ClinVar RCV Id: RCV000055557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ala1498_Ile1503del
CA022183
NM_001318831.2:c.4492_4509del