Canonical Allele Identifier: PA2830111120
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 2925650
ClinVar RCV Id: RCV003783744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116780.1:p.Arg530Gln
CA9778414
NM_032985.6:c.1589G>A