Canonical Allele Identifier: PA2825574556
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467940

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Arg799Cys
CA394277095
NM_001114382.3:c.2395C>T