Canonical Allele Identifier: PA915986916
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Arg316Trp
CA039888
NM_001162426.2:c.946C>T