Canonical Allele Identifier: PA916073972
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 532197
ClinVar RCV Id: RCV000638851 RCV001509052
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116781.1:p.Glu439Asp
CA9778320
NM_032986.5:c.1317G>T
CA408363116
NM_032986.5:c.1317G>C