Canonical Allele Identifier: PA2825957907
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411222

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Ala1019Val
CA16612440
NM_001162427.2:c.3056C>T