Canonical Allele Identifier: PA2827003156
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1728211
ClinVar RCV Id: RCV002320843
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Leu971Arg
CA394285304
NM_001318827.2:c.2912T>G