Canonical Allele Identifier: PA109895
Gene: NCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 30194
ClinVar RCV Id: RCV000023113 RCV000208606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000622.2:p.Arg105Gln
CA129011
NM_000631.5:c.314G>A