Canonical Allele Identifier: PA2827014928
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535925

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Arg1085Cys
CA049839
NM_001318831.2:c.3253C>T