Canonical Allele Identifier: PA915987457
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 379061

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Ala975Thr
CA035755
NM_001162427.2:c.2923G>A