Canonical Allele Identifier: PA2827008227
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Arg868Gln
CA018086
NM_001318829.2:c.2603G>A