Canonical Allele Identifier: PA2825956929
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 820805

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Arg667Trp
CA375360858
NM_001162427.2:c.1999C>T