Canonical Allele Identifier: PA2827010436
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1359198
ClinVar RCV Id: RCV001904352

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.His1631Arg
CA394314615
NM_001318829.2:c.4892A>G