Canonical Allele Identifier: PA2828409909
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Lys69Glu
CA036103
NM_001370404.1:c.205A>G