Allele Registry

Canonical Allele Identifier: PA2826164563

Gene: NCF2 HGNC NCBI

ClinVar RCV:

RCV000243467

RCV000388595

RCV001651127

ClinVar Variation:

256116

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177723.1:p.Lys136Arg	CA1284929 NM_001190794.2:c.407A>G