Canonical Allele Identifier: PA2826164382
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_001177718.1:p.Gly288Arg
CA219764
NM_001190789.2:c.862G>A
CA343704591
NM_001190789.2:c.862G>C