Canonical Allele Identifier: PA2825574128
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535981

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Arg680Leu
CA394274563
NM_001114382.3:c.2039G>T