Canonical Allele Identifier: PA2829657496
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 2533497
ClinVar RCV Id: RCV003291207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006354.2:p.Gly305Arg
CA9778164
NM_006363.6:c.913G>A
CA408360182
NM_006363.6:c.913G>C