Canonical Allele Identifier: PA103529
Gene: CYBB HGNC NCBI

Linked Data

ClinVar Variation Id: 68406
ClinVar RCV Id: RCV000059273
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000388.2:p.Ala224Gly
CA219746
NM_000397.4:c.671C>G