Canonical Allele Identifier: PA2825212645
Gene: NCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 642515
ClinVar RCV Id: RCV000795993
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000622.2:p.Phe41Tyr
CA411378599
NM_000631.5:c.122T>A