Allele Registry

Canonical Allele Identifier: PA2826164691

Gene: NCF2 HGNC NCBI

ClinVar RCV:

RCV000002336

RCV000597800

RCV001650826

RCV003603847

ClinVar Variation:

2248

2910829

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177723.1:p.Arg350Trp	CA115437 NM_001190794.2:c.1048C>T CA2739275464 NM_001190794.2:c.1047_1048delinsCT