Canonical Allele Identifier: PA916043256
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 49073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Phe95Ser
CA007933
NM_001362177.1:c.284T>C