Canonical Allele Identifier: PA658659846
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466116

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Pro1023Leu
CA375367614
NM_000368.5:c.3068C>T