Canonical Allele Identifier: PA658659684
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466054

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Ala659Thr
CA200888114
NM_000368.5:c.1975G>A