Canonical Allele Identifier: PA2829657517
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 2102765
ClinVar RCV Id: RCV003037784 RCV004550350
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006354.2:p.Ala329Pro
CA9778177
NM_006363.6:c.985G>C