Canonical Allele Identifier: PA2825575520
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535973

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Arg1129His
CA394286758
NM_001114382.3:c.3386G>A