Canonical Allele Identifier: PA2826079750
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 1438971
ClinVar RCV Id: RCV001934399
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166217.1:p.Asp288Asn
CA9778165
NM_001172746.3:c.862G>A