Canonical Allele Identifier: PA2827012795
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65084

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Arg385His
CA015651
NM_001318831.2:c.1154G>A