Canonical Allele Identifier: PA2825957642
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411234

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Ala893Thr
CA034791
NM_001162427.2:c.2677G>A