Canonical Allele Identifier: PA2828419810
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1374125
ClinVar RCV Id: RCV001877669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ser1178Thr
CA394292074
NM_001370405.1:c.3532T>A