Canonical Allele Identifier: PA915997292
Gene: NCF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2247
ClinVar RCV Id: RCV000002335
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177723.1:p.Arg77Gln
CA115435
NM_001190794.2:c.230G>A