Canonical Allele Identifier: PA2827011847
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3073959
ClinVar RCV Id: RCV004012501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Thr983Pro
CA394285967
NM_001318829.2:c.2947A>C