Canonical Allele Identifier: PA2828059817
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 41690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Ser366Cys
CA004868
NM_001362177.1:c.1097C>G