Canonical Allele Identifier: PA109028
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 1222
ClinVar RCV Id: RCV000001281 RCV000081407 RCV000688348 RCV004547453
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166216.1:p.Glu109Lys
CA114843
NM_001172745.3:c.325G>A