Canonical Allele Identifier: PA658677170
Gene: CYBB HGNC NCBI

Linked Data

ClinVar Variation Id: 450082
ClinVar RCV Id: RCV001696923

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000388.2:p.Ala49Thr
CA412972700
NM_000397.4:c.145G>A