Canonical Allele Identifier: PA2827020109
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 387484
ClinVar RCV Id: RCV001088704 RCV000442144 RCV002328973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Pro1461Thr
CA16606959
NM_001318832.2:c.4381C>A