Canonical Allele Identifier: PA2827002866
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1795250
ClinVar RCV Id: RCV002431341
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Pro873Ile
CA2580090869
NM_001318827.2:c.2617_2618delinsAT