Canonical Allele Identifier: PA645413147
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Thr300Ile
CA039371
NM_000368.5:c.899C>T