Canonical Allele Identifier: PA2825955443
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3231338
ClinVar RCV Id: RCV004525409
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Leu266Pro
CA375368697
NM_001162427.2:c.797T>C