Canonical Allele Identifier: PA2825956605
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411257

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Gly588Val
CA030103
NM_001162427.2:c.1763G>T