Canonical Allele Identifier: PA2825439424
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406029

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Arg1646Cys
CA054033
NM_001077183.3:c.4936C>T