Canonical Allele Identifier: PA104035
Gene: CYBB HGNC NCBI

Linked Data

ClinVar Variation Id: 68396
ClinVar RCV Id: RCV000059262
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000388.2:p.Ser193Phe
CA219724
NM_000397.4:c.578C>T