Canonical Allele Identifier: PA2827009834
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49310

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Glu1437del
CA020824
NM_001318829.2:c.4310_4312del