Canonical Allele Identifier: PA916043210
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 64837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Phe37Ser
CA007609
NM_001362177.1:c.110T>C