Canonical Allele Identifier: PA2827016010
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207757

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Arg1390Cys
CA053034
NM_001318831.2:c.4168C>T