Canonical Allele Identifier: PA2827020241
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49310
ClinVar RCV Id: RCV000042570 RCV000691590 RCV002336157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Glu1496del
CA020824
NM_001318832.2:c.4487_4489del