Allele Registry

Canonical Allele Identifier: PA915968084

Gene: NCF2 HGNC NCBI

ClinVar RCV:

RCV000526618

RCV001532089

RCV002282216

ClinVar Variation:

466297

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121123.1:p.Thr361Ser	CA1284684 NM_001127651.3:c.1081A>T