Allele Registry

Canonical Allele Identifier: PA2826078744

Gene: SEC23B HGNC NCBI

ClinVar RCV:

RCV000179916

RCV000329540

RCV001509924

RCV004553017

ClinVar Variation:

198541

HGVS (amino-acid)	Matching Registered Transcripts
NP_001166216.1:p.Gln258Arg	CA247249 NM_001172745.3:c.773A>G