Canonical Allele Identifier: PA2825439522
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 661952

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ile1668Thr
CA276759442
NM_001077183.3:c.5003T>C