Canonical Allele Identifier: PA2827020950
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65333
ClinVar RCV Id: RCV000055557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ala1686_Ile1691del
CA022183
NM_001318832.2:c.5056_5073del