Canonical Allele Identifier: PA2828061076
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 486574

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Met883Thr
CA035603
NM_001362177.1:c.2648T>C