Canonical Allele Identifier: PA2827014355
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406055

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Arg834Gln
CA044900
NM_001318831.2:c.2501G>A