Canonical Allele Identifier: PA2829977645
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486602
ClinVar RCV Id: RCV000562822 RCV001049308 RCV004001145
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Thr927Ile
CA394279934
NM_021055.3:c.2780C>T