Canonical Allele Identifier: PA2827002893
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467964
ClinVar RCV Id: RCV000554781 RCV002438413 RCV003999276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Arg880Trp
CA041738
NM_001318827.2:c.2638C>T