Canonical Allele Identifier: PA2829980252
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 954178
ClinVar RCV Id: RCV001226591 RCV002356962 RCV002491716
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Glu1301Gly
CA394299251
NM_021055.3:c.3902A>G