Canonical Allele Identifier: PA2825575183
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 386865
ClinVar RCV Id: RCV000433002 RCV000456443 RCV002323631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Met1030Val
CA044156
NM_001114382.3:c.3088A>G