Canonical Allele Identifier: PA2825954946
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 64837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Phe107Ser
CA007609
NM_001162427.2:c.320T>C