Canonical Allele Identifier: PA2827002526
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49725
ClinVar RCV Id: RCV000042990 RCV000189999 RCV000201105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Cys767Arg
CA017384
NM_001318827.2:c.2299T>C