Canonical Allele Identifier: PA2826164522
Gene: NCF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2082303
ClinVar RCV Id: RCV002995921
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177723.1:p.Asp34Gly
CA1285059
NM_001190794.2:c.101A>G