Canonical Allele Identifier: PA2827007678
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 186667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Arg669His
CA016838
NM_001318829.2:c.2006G>A