Canonical Allele Identifier: PA103585
Gene: CYBB HGNC NCBI

Linked Data

ClinVar Variation Id: 68388
ClinVar RCV Id: RCV000059250

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000388.2:p.Arg54Ser
CA219708
NM_000397.4:c.162G>C
CA412972732
NM_000397.4:c.162G>T