Canonical Allele Identifier: PA2827011797
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406049
ClinVar RCV Id: RCV000467462
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Thr976Pro
CA16615089
NM_001318829.2:c.2926A>C