Canonical Allele Identifier: PA658659901
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Leu1117Pro
CA036590
NM_000368.5:c.3350T>C