Canonical Allele Identifier: PA2828059234
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1692412
ClinVar RCV Id: RCV002257190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Glu137Val
CA375369591
NM_001362177.1:c.410A>T