Canonical Allele Identifier: PA2825956175
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 377283

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Ser529Thr
CA029137
NM_001162426.2:c.1586G>C