Canonical Allele Identifier: PA103871
Gene: CYBB HGNC NCBI

Linked Data

ClinVar Variation Id: 68402
ClinVar RCV Id: RCV000059269
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000388.2:p.His222Tyr
CA219736
NM_000397.4:c.664C>T