Allele Registry

Canonical Allele Identifier: PA115439

Gene: NCF2 HGNC NCBI

ClinVar RCV:

RCV000002336

RCV000597800

RCV001650826

RCV003603847

ClinVar Variation:

2248

2910829

HGVS (amino-acid)	Matching Registered Transcripts
NP_000424.2:p.Arg395Trp	CA115437 NM_000433.4:c.1183C>T CA2739275464 NM_000433.4:c.1182_1183delinsCT