Canonical Allele Identifier: PA2828413089
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406074
ClinVar RCV Id: RCV000470486 RCV002323694 RCV004000713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ala1009Val
CA044608
NM_001370404.1:c.3026C>T