Canonical Allele Identifier: PA2827001888
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406001
ClinVar RCV Id: RCV000473625 RCV000570501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Asp598Asn
CA16615059
NM_001318827.2:c.1792G>A