Canonical Allele Identifier: PA2573170602
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1359198
ClinVar RCV Id: RCV001904352

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.His1746Arg
CA394314615
NM_000548.5:c.5237A>G