Canonical Allele Identifier: PA2825955791
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411231

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Pro367His
CA16612640
NM_001162427.2:c.1100C>A