Canonical Allele Identifier: PA2826078822
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 2337568
ClinVar RCV Id: RCV002949867
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166216.1:p.Ala323Ser
CA9778172
NM_001172745.3:c.967G>T