Canonical Allele Identifier: PA2825957475
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411268

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Val844Ile
CA034261
NM_001162427.2:c.2530G>A