Canonical Allele Identifier: PA2828416861
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468193
ClinVar RCV Id: RCV000541726 RCV002377105 RCV003999344
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Val319Met
CA394315689
NM_001370405.1:c.955G>A