Canonical Allele Identifier: PA2827005611
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1006099
ClinVar RCV Id: RCV001303092
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.His1666Gln
CA394315387
NM_001318827.2:c.4998C>A
CA394315391
NM_001318827.2:c.4998C>G