Canonical Allele Identifier: PA2828421659
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65333
ClinVar RCV Id: RCV000055557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ala1695_Ile1700del
CA022183
NM_001370405.1:c.5083_5100del