Canonical Allele Identifier: PA2827004752
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 847208
ClinVar RCV Id: RCV001050709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Lys1441Arg
CA394304865
NM_001318827.2:c.4322A>G