Canonical Allele Identifier: PA2830110880
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 1438971
ClinVar RCV Id: RCV001934399
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116780.1:p.Asp306Asn
CA9778165
NM_032985.6:c.916G>A