Canonical Allele Identifier: PA2828413406
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207784
ClinVar RCV Id: RCV000190077 RCV000644198 RCV002453704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Leu1098Pro
CA319595
NM_001370404.1:c.3293T>C