Canonical Allele Identifier: PA129013
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_038202.2:p.Arg105Gln
CA129011
NM_013416.4:c.314G>A