Allele Registry

Canonical Allele Identifier: PA2826164694

Gene: NCF2 HGNC NCBI

ClinVar RCV:

RCV001212887

ClinVar Variation:

942822

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177723.1:p.Arg350Gly	CA1284646 NM_001190794.2:c.1048C>G