Canonical Allele Identifier: PA2827013759
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Glu645Gly
CA039405
NM_001318831.2:c.1934A>G