Canonical Allele Identifier: PA2828059685
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 135362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Ala307Leu
CA004602
NM_001362177.1:c.919_920delinsCT