Allele Registry

Canonical Allele Identifier: PA916073954

Gene: SEC23B HGNC NCBI

ClinVar Allele:

195702

ClinVar RCV:

RCV000179916

RCV000329540

RCV001509924

RCV004553017

ClinVar Variation:

198541

HGVS (amino-acid)	Matching Registered Transcripts
NP_116781.1:p.Gln258Arg	CA247249 NM_032986.5:c.773A>G