Canonical Allele Identifier: PA658806702
Gene: NCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 539179
ClinVar RCV Id: RCV000648868 RCV000728333 RCV003987645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_038202.2:p.Arg60His
CA10212884
NM_013416.4:c.179G>A