Canonical Allele Identifier: PA915987374
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 486592

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Gln98Glu
CA375373395
NM_001162427.2:c.292C>G