Canonical Allele Identifier: PA2826079740
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 3064761
ClinVar RCV Id: RCV003989246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166217.1:p.Gly283Asp
CA408360158
NM_001172746.3:c.848G>A