Canonical Allele Identifier: PA2825169994
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_000424.2:p.Asp34Gly
CA1285059
NM_000433.4:c.101A>G