Canonical Allele Identifier: PA2827001800
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1780872
ClinVar RCV Id: RCV002410465 RCV003100868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Ile573Leu
CA394273001
NM_001318827.2:c.1717A>C