Canonical Allele Identifier: PA2827013326
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 186667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Arg518His
CA016838
NM_001318831.2:c.1553G>A