Canonical Allele Identifier: PA2828059401
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Arg195Trp
CA039888
NM_001362177.1:c.583C>T