Canonical Allele Identifier: PA2825955059
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 49060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Leu140His
CA007782
NM_001162427.2:c.419T>A