Canonical Allele Identifier: PA2825955124
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1753832
ClinVar RCV Id: RCV002356248

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Phe165Leu
CA375371683
NM_001162427.2:c.495T>G
CA375371686
NM_001162427.2:c.495T>A
CA375371696
NM_001162427.2:c.493T>C