Canonical Allele Identifier: PA2828412727
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_001357333.1:p.Val892Ile
CA276741706
NM_001370404.1:c.2674G>A