Canonical Allele Identifier: PA2826079746
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 2533497
ClinVar RCV Id: RCV003291207
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166217.1:p.Gly287Arg
CA9778164
NM_001172746.3:c.859G>A
CA408360182
NM_001172746.3:c.859G>C