Canonical Allele Identifier: PA222938
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 95384
ClinVar RCV Id: RCV000081403 RCV001843475 RCV003764767
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006354.2:p.Ala524Val
CA222937
NM_006363.6:c.1571C>T