Canonical Allele Identifier: PA2827015228
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535982

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Arg1173Trp
CA050704
NM_001318831.2:c.3517C>T