Canonical Allele Identifier: PA915986822
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411277

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Pro286Arg
CA039224
NM_001162426.2:c.857C>G