Canonical Allele Identifier: PA2826078824
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 1226
ClinVar RCV Id: RCV000001285 RCV002512638 RCV003137483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166216.1:p.Arg324Ter