Canonical Allele Identifier: PA645466590
Gene: NCF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 294081
ClinVar RCV Id: RCV000973778 RCV001709577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000424.2:p.Arg386Gln
CA1284671
NM_000433.4:c.1157G>A