Canonical Allele Identifier: PA2825577098
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1519622
ClinVar RCV Id: RCV002038344 RCV002331644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ala1594Val
CA394308216
NM_001114382.3:c.4781C>T