Canonical Allele Identifier: PA2827001942
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2711441
ClinVar RCV Id: RCV003513095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Tyr611His
CA394273393
NM_001318827.2:c.1831T>C