Canonical Allele Identifier: PA2829976981
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467951
ClinVar RCV Id: RCV000552388 RCV001770442 RCV002456153 RCV003999272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Pro854Leu
CA394278313
NM_021055.3:c.2561C>T