Canonical Allele Identifier: PA2828421777
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_001357334.1:p.His1722Gln
CA394315387
NM_001370405.1:c.5166C>A
CA394315391
NM_001370405.1:c.5166C>G