Canonical Allele Identifier: PA2826079759
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 2925648
ClinVar RCV Id: RCV003783742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166217.1:p.Ile300Thr
CA312396298
NM_001172746.3:c.899T>C