Canonical Allele Identifier: PA2827010641
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_001305758.1:p.Ile1682dup
CA2580091208
NM_001318829.2:c.5044_5046dup