Canonical Allele Identifier: PA2825958060
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 184790

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Asp1085Glu
CA007356
NM_001162427.2:c.3255T>A
CA375366432
NM_001162427.2:c.3255T>G