Allele Registry

Canonical Allele Identifier: PA916073987

Gene: SEC23B HGNC NCBI

ClinVar RCV:

RCV000001283

RCV003480015

RCV003764507

ClinVar Variation:

1224

HGVS (amino-acid)	Matching Registered Transcripts
NP_116781.1:p.Arg530Trp	CA114849 NM_032986.5:c.1588C>T