Canonical Allele Identifier: PA2825435598
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2626418
ClinVar RCV Id: RCV003382398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Thr521Ile
CA394326548
NM_001077183.3:c.1562C>T