Canonical Allele Identifier: PA2827016690
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1977864
ClinVar RCV Id: RCV002736837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ile1553dup
CA2580091208
NM_001318831.2:c.4657_4659dup