Canonical Allele Identifier: PA915987347
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 184670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Val76Ile
CA007499
NM_001162427.2:c.226G>A