Canonical Allele Identifier: PA2826164231
Gene: NCF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 947988
ClinVar RCV Id: RCV001219158
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177718.1:p.Met53Val
CA33992941
NM_001190789.2:c.157A>G