Canonical Allele Identifier: PA658816602
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 532197
ClinVar RCV Id: RCV000638851 RCV001509052
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006354.2:p.Glu439Asp
CA9778320
NM_006363.6:c.1317G>T
CA408363116
NM_006363.6:c.1317G>C