Allele Registry

Canonical Allele Identifier: PA2826164376

Gene: NCF2 HGNC NCBI

ClinVar RCV:

RCV000526618

RCV001532089

RCV002282216

ClinVar Variation:

466297

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177718.1:p.Thr280Ser	CA1284684 NM_001190789.2:c.838A>T