Canonical Allele Identifier: PA2829982422
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207757
ClinVar RCV Id: RCV000725350 RCV001314556 RCV002336506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Arg1591Cys
CA053034
NM_021055.3:c.4771C>T