Allele Registry

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Canonical Allele Identifier: PA2828411400

Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3232082

ClinVar RCV Id: RCV004518797

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357333.1:p.Ser526Arg	CA394326663 NM_001370404.1:c.1576A>C CA394326680 NM_001370404.1:c.1578C>A CA394326682 NM_001370404.1:c.1578C>G