Canonical Allele Identifier: PA2829657667
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 2925650
ClinVar RCV Id: RCV003783744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006354.2:p.Arg530Gln
CA9778414
NM_006363.6:c.1589G>A