Canonical Allele Identifier: PA2827020213
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 838523
ClinVar RCV Id: RCV001040088 RCV001813810 RCV002339198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ile1489Met
CA394304898
NM_001318832.2:c.4467C>G