Canonical Allele Identifier: PA2825954837
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 49069
ClinVar RCV Id: RCV000042322
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Ser201del
CA007876
NM_001162426.2:c.602_604del