Canonical Allele Identifier: PA114847
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 1223
ClinVar RCV Id: RCV000001282 RCV000153924 RCV000688744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006354.2:p.Arg14Trp
CA114846
NM_006363.6:c.40C>T