Canonical Allele Identifier: PA2826079060
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_001166216.1:p.Arg497Cys
CA234906
NM_001172745.3:c.1489C>T