Canonical Allele Identifier: PA247251
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 198541
ClinVar RCV Id: RCV000179916 RCV000329540 RCV001509924 RCV004553017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116780.1:p.Gln258Arg
CA247249
NM_032985.6:c.773A>G