Canonical Allele Identifier: PA658659760
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 486590

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Thr874Pro
CA375369840
NM_000368.5:c.2620A>C