Canonical Allele Identifier: PA2828409898
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_001357333.1:p.Val67Ile
CA035477
NM_001370404.1:c.199G>A