Canonical Allele Identifier: PA2828094891
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65243
ClinVar RCV Id: RCV000055464 RCV000590930 RCV002513723
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.His1554Arg
CA021150
NM_001363528.2:c.4661A>G