Canonical Allele Identifier: PA2827002844
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2762661
ClinVar RCV Id: RCV003512525
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Pro866Leu
CA394279468
NM_001318827.2:c.2597C>T