Canonical Allele Identifier: PA2828094583
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 963446
ClinVar RCV Id: RCV001237474
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Leu1468Val
CA394304603
NM_001363528.2:c.4402C>G