Canonical Allele Identifier: PA2827004711
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49308
ClinVar RCV Id: RCV000042567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Leu1431His
CA020740
NM_001318827.2:c.4292T>A