Canonical Allele Identifier: PA2825571961
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467862
ClinVar RCV Id: RCV000543191 RCV002384164 RCV004527645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Leu45Arg
CA394301803
NM_001114382.3:c.134T>G