Canonical Allele Identifier: PA2827005489
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65333
ClinVar RCV Id: RCV000055557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Ala1639_Ile1644del
CA022183
NM_001318827.2:c.4915_4932del