Canonical Allele Identifier: PA2825436083
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Lys658Thr
CA016374
NM_001077183.3:c.1973A>C