Canonical Allele Identifier: PA2825439544
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65333
ClinVar RCV Id: RCV000055557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ala1675_Ile1680del
CA022183
NM_001077183.3:c.5023_5040del