Canonical Allele Identifier: PA2825956332
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Thr523Ser
CA029589
NM_001162427.2:c.1568C>G
CA375363989
NM_001162427.2:c.1567A>T