Allele Registry

Canonical Allele Identifier: PA2825170191

Gene: NCF2 HGNC NCBI

ClinVar RCV:

RCV001212887

ClinVar Variation:

942822

HGVS (amino-acid)	Matching Registered Transcripts
NP_000424.2:p.Arg395Gly	CA1284646 NM_000433.4:c.1183C>G