Canonical Allele Identifier: PA2827000854
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65217
ClinVar RCV Id: RCV000055437 RCV001730486 RCV002381358
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Val297Ala
CA013517
NM_001318827.2:c.890T>C