Canonical Allele Identifier: PA2826079928
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 167667
ClinVar RCV Id: RCV000153928 RCV000779341 RCV001850108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166217.1:p.Arg479Cys
CA234906
NM_001172746.3:c.1435C>T