Canonical Allele Identifier: PA2829979755
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230769

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Pro1222del
CA10579895
NM_021055.3:c.3665_3667del