Canonical Allele Identifier: PA2829657666
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 1224
ClinVar RCV Id: RCV000001283 RCV003480015 RCV003764507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006354.2:p.Arg530Trp
CA114849
NM_006363.6:c.1588C>T