Canonical Allele Identifier: PA915986609
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 231802

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Val96Ala
CA034878
NM_001162426.2:c.287T>C