Canonical Allele Identifier: PA2827013956
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Arg705Gly
CA017936
NM_001318831.2:c.2113C>G