Canonical Allele Identifier: PA2830110876
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 3064761
ClinVar RCV Id: RCV003989246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116780.1:p.Gly301Asp
CA408360158
NM_032985.6:c.902G>A