Allele Registry

Canonical Allele Identifier: PA645505901

Gene: NCF2 HGNC NCBI

ClinVar RCV:

RCV000243467

RCV000388595

RCV001651127

ClinVar Variation:

256116

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121123.1:p.Lys181Arg	CA1284929 NM_001127651.3:c.542A>G