Canonical Allele Identifier: PA915976266
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467980
ClinVar RCV Id: RCV000530166 RCV002255448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Arg988His
CA043038
NM_001114382.3:c.2963G>A