Canonical Allele Identifier: PA2827002696
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237996
ClinVar RCV Id: RCV000230556 RCV001091442 RCV002429101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Tyr820Cys
CA10583311
NM_001318827.2:c.2459A>G