Allele Registry

Canonical Allele Identifier: PA234905

Gene: SEC23B HGNC NCBI

ClinVar RCV:

RCV000153925

RCV000490449

RCV001082004

RCV001335411

ClinVar Variation:

167665

HGVS (amino-acid)	Matching Registered Transcripts
NP_116780.1:p.Pro25His	CA234903 NM_032985.6:c.74C>A