Canonical Allele Identifier: PA2827012591
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64901

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Leu328Pro
CA015160
NM_001318831.2:c.983T>C