Canonical Allele Identifier: PA2825958022
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Leu1066Pro
CA036590
NM_001162427.2:c.3197T>C