Canonical Allele Identifier: PA916043221
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411271

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Val51Met
CA16612590
NM_001362177.1:c.151G>A