Canonical Allele Identifier: PA107566
Gene: NCF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2247
ClinVar RCV Id: RCV000002335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000424.2:p.Arg77Gln
CA115435
NM_000433.4:c.230G>A