Canonical Allele Identifier: PA2826857713
Gene: CCDC28B HGNC NCBI

Linked Data

ClinVar Variation Id: 373579
ClinVar RCV Id: RCV000412925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287940.1:p.Gly94Glu
CA739189
NM_001301011.2:c.281G>A