Canonical Allele Identifier: PA915987204
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207623

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Lys30Arg
CA319269
NM_001162427.2:c.89A>G