Canonical Allele Identifier: PA2827015539
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Gln1259Pro
CA020573
NM_001318831.2:c.3776A>C