Allele Registry

Canonical Allele Identifier: PA1139679841

Gene: NCF2 HGNC NCBI

ClinVar RCV:

RCV001212887

ClinVar Variation:

942822

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121123.1:p.Arg395Gly	CA1284646 NM_001127651.3:c.1183C>G