Canonical Allele Identifier: PA2825212666
Gene: NCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 500837
ClinVar RCV Id: RCV000595538 RCV000968901 RCV001509096 RCV003905544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000622.2:p.Arg58Cys
CA10212881
NM_000631.5:c.172C>T