Canonical Allele Identifier: PA2825577552
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405952
ClinVar RCV Id: RCV000467027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Thr1710del
CA16615195
NM_001114382.3:c.5128_5133delinsGAC
CA2575877453
NM_001114382.3:c.5128_5130del