Canonical Allele Identifier: PA2828059687
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 486593

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Ala307Val
CA375366183
NM_001362177.1:c.920C>T