Canonical Allele Identifier: PA234904
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 167665
ClinVar RCV Id: RCV000153925 RCV000490449 RCV001082004 RCV001335411
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006354.2:p.Pro25His
CA234903
NM_006363.6:c.74C>A