Allele Registry

Canonical Allele Identifier: PA2826164398

Gene: NCF2 HGNC NCBI

ClinVar RCV:

RCV001212887

ClinVar Variation:

942822

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177718.1:p.Arg314Gly	CA1284646 NM_001190789.2:c.940C>G