Canonical Allele Identifier: PA645413571
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411228

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Pro1140Leu
CA036899
NM_000368.5:c.3419C>T