Canonical Allele Identifier: PA2829983251
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406029
ClinVar RCV Id: RCV000466636 RCV002348293
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Arg1670Cys
CA054033
NM_021055.3:c.5008C>T