Canonical Allele Identifier: PA2827011528
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535858
ClinVar RCV Id: RCV000644069 RCV002424462 RCV004003985
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Val843Ile
CA276741706
NM_001318829.2:c.2527G>A