Canonical Allele Identifier: PA2825212663
Gene: NCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 853519
ClinVar RCV Id: RCV001058342
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000622.2:p.Arg57Leu
CA10212879
NM_000631.5:c.170G>T