Canonical Allele Identifier: PA916073988
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 767195

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116781.1:p.Gly532Ala
CA9778415
NM_032986.5:c.1595G>C