Canonical Allele Identifier: PA2827012831
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49173

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.His393Arg
CA015696
NM_001318831.2:c.1178A>G