Canonical Allele Identifier: PA2829970569
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_066399.2:p.Lys69Glu
CA036103
NM_021055.3:c.205A>G