Canonical Allele Identifier: PA2829983639
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3232189
ClinVar RCV Id: RCV004520872

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.His1703Tyr
CA394314606
NM_021055.3:c.5107C>T