Allele Registry

Canonical Allele Identifier: PA2826079821

Gene: SEC23B HGNC NCBI

ClinVar Variation Id: 337792

HGVS (amino-acid)	Matching Registered Transcripts
NP_001166217.1:p.Phe382Leu	CA9778252 NM_001172746.3:c.1144T>C CA408361773 NM_001172746.3:c.1146C>A CA408361775 NM_001172746.3:c.1146C>G