Canonical Allele Identifier: PA658659420
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 448716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Pro114Ser
CA036801
NM_000368.5:c.340C>T