Canonical Allele Identifier: PA916023180
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Lys45Arg
CA027990
NM_001318832.2:c.134A>G