Canonical Allele Identifier: PA2826078800
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 3064761
ClinVar RCV Id: RCV003989246
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166216.1:p.Gly301Asp
CA408360158
NM_001172745.3:c.902G>A