Canonical Allele Identifier: PA2829983463
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405952
ClinVar RCV Id: RCV000467027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Thr1690del
CA16615195
NM_021055.3:c.5068_5073delinsGAC
CA2575877453
NM_021055.3:c.5068_5070del