Canonical Allele Identifier: PA2828410660
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 283532
ClinVar RCV Id: RCV000394048 RCV000570041 RCV001089419
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Phe298Ser
CA056651
NM_001370404.1:c.893T>C