Canonical Allele Identifier: PA2829983631
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405943
ClinVar RCV Id: RCV000595657 RCV000768353 RCV001085143 RCV001023772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Arg1702Cys
CA054522
NM_021055.3:c.5104C>T