Canonical Allele Identifier: PA2827015356
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535857
ClinVar Variation Id: 1057663

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ser1210Arg
CA394301651
NM_001318831.2:c.3628A>C
CA394301677
NM_001318831.2:c.3630T>A
CA394301688
NM_001318831.2:c.3630T>G