Canonical Allele Identifier: PA658659492
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 486585

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Pro231Leu
CA375371402
NM_000368.5:c.692C>T