Canonical Allele Identifier: PA2827000160
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535919
ClinVar RCV Id: RCV000644149 RCV003303040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Lys69Glu
CA036103
NM_001318827.2:c.205A>G