Canonical Allele Identifier: PA645466562
Gene: NCF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 287151
ClinVar RCV Id: RCV000313929 RCV001085219 RCV002222475 RCV003949889
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000424.2:p.Arg38Gln
CA1285055
NM_000433.4:c.113G>A