Canonical Allele Identifier: PA2828061164
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 41696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Gly914Ser
CA007165
NM_001362177.1:c.2740G>A