Canonical Allele Identifier: PA2827010677
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535927
ClinVar RCV Id: RCV000644157 RCV002422324 RCV004004003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Val18Ile
CA035477
NM_001318829.2:c.52G>A