Allele Registry

Canonical Allele Identifier: PA109028

Gene: SEC23B HGNC NCBI

ClinVar RCV:

RCV000001281

RCV000081407

RCV000688348

RCV004547453

ClinVar Variation:

1222

HGVS (amino-acid)	Matching Registered Transcripts
NP_001166216.1:p.Glu109Lys	CA114843 NM_001172745.3:c.325G>A