Canonical Allele Identifier: PA2825957064
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466072

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Tyr710His
CA032032
NM_001162427.2:c.2128T>C