Canonical Allele Identifier: PA2825212696
Gene: NCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1507422
ClinVar RCV Id: RCV002009479
ClinVar Variation Id: 2636889
ClinVar RCV Id: RCV003421076 RCV003641094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000622.2:p.Gly74Arg
CA10212889
NM_000631.5:c.220G>A
CA323985750
NM_000631.5:c.220G>C