Canonical Allele Identifier: PA2825955699
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411241

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Tyr405Cys
CA027303
NM_001162426.2:c.1214A>G