Canonical Allele Identifier: PA645375768
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_077272.2:p.Gly94Glu
CA739189
NM_024296.5:c.281G>A