Canonical Allele Identifier: PA915986887
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 800246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Ala307Val
CA039745
NM_001162426.2:c.920C>T