Canonical Allele Identifier: PA2827015630
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 825015
ClinVar RCV Id: RCV001022728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ser1282Thr
CA394304356
NM_001318831.2:c.3844T>A