Canonical Allele Identifier: PA2825955121
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 49073
ClinVar RCV Id: RCV000042326 RCV000641989
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Phe165Ser
CA007933
NM_001162427.2:c.494T>C