Canonical Allele Identifier: PA2829983138
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65364
ClinVar RCV Id: RCV000055589 RCV002345361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Leu1665Pro
CA021783
NM_021055.3:c.4994T>C