Canonical Allele Identifier: PA2829657485
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 2435795
ClinVar RCV Id: RCV003136545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006354.2:p.Thr292Ile
CA408360109
NM_006363.6:c.875C>T