Canonical Allele Identifier: PA2827008979
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230769

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Pro1173del
CA10579895
NM_001318829.2:c.3518_3520del