Canonical Allele Identifier: PA2829983637
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1359198
ClinVar RCV Id: RCV001904352

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.His1703Arg
CA394314615
NM_021055.3:c.5108A>G