Canonical Allele Identifier: PA2827012778
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1408964
ClinVar RCV Id: RCV001909636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ser381Cys
CA394272745
NM_001318831.2:c.1141A>T