Canonical Allele Identifier: PA915986821
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 64699

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Phe285Val
CA008327
NM_001162426.2:c.853T>G