Canonical Allele Identifier: PA2827002948
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49233
ClinVar RCV Id: RCV000042492 RCV000556585 RCV002433524
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Phe896Cys
CA018204
NM_001318827.2:c.2687T>G