Canonical Allele Identifier: PA2825956497
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411213

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Val593Glu
CA16612455
NM_001162426.2:c.1778T>A