Canonical Allele Identifier: PA2829981827
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_066399.2:p.Glu1509del
CA020824
NM_021055.3:c.4526_4528del