Canonical Allele Identifier: PA2829981482
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468092
ClinVar RCV Id: RCV000546695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Gln1460Arg
CA394302741
NM_021055.3:c.4379A>G