Canonical Allele Identifier: PA2826164221
Gene: NCF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 287151
ClinVar RCV Id: RCV000313929 RCV001085219 RCV002222475 RCV003949889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177718.1:p.Arg38Gln
CA1285055
NM_001190789.2:c.113G>A