Canonical Allele Identifier: PA2827005535
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207760

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Arg1648His
CA054581
NM_001318827.2:c.4943G>A