Canonical Allele Identifier: PA645510497
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 337792
ClinVar RCV Id: RCV000275527 RCV000945938 RCV001509049 RCV004549773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006354.2:p.Phe400Leu
CA9778252
NM_006363.6:c.1198T>C
CA408361773
NM_006363.6:c.1200C>A
CA408361775
NM_006363.6:c.1200C>G