Canonical Allele Identifier: PA2825919500
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207644

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Arg1096Cys
CA036377
NM_001162426.2:c.3286C>T