Canonical Allele Identifier: PA2827004788
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 953372
ClinVar RCV Id: RCV001225656 RCV001664766
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Gly1450Asp
CA394305086
NM_001318827.2:c.4349G>A