Canonical Allele Identifier: PA2580465823
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 2337568
ClinVar RCV Id: RCV002949867
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116781.1:p.Ala323Ser
CA9778172
NM_032986.5:c.967G>T