Canonical Allele Identifier: PA2825958073
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1431901
ClinVar RCV Id: RCV001959735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Pro1089Ser
CA375366412
NM_001162427.2:c.3265C>T