Canonical Allele Identifier: PA915997271
Gene: NCF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 641200
ClinVar RCV Id: RCV000794385 RCV004027485
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177723.1:p.Arg38Trp
CA1285056
NM_001190794.2:c.112C>T