Canonical Allele Identifier: PA2828414156
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405949
ClinVar RCV Id: RCV000713932 RCV002257693 RCV001086293
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Val1319Ile
CA050403
NM_001370404.1:c.3955G>A