Canonical Allele Identifier: PA219766
Gene: NCF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 68484
ClinVar RCV Id: RCV000059356 RCV001854241
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000424.2:p.Gly369Arg
CA219764
NM_000433.4:c.1105G>A
CA343704591
NM_000433.4:c.1105G>C