Allele Registry

Canonical Allele Identifier: PA916073931

Gene: SEC23B HGNC NCBI

ClinVar RCV:

RCV000001282

RCV000153924

RCV000688744

ClinVar Variation:

1223

HGVS (amino-acid)	Matching Registered Transcripts
NP_116781.1:p.Arg14Trp	CA114846 NM_032986.5:c.40C>T