Canonical Allele Identifier: PA2825648803
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_001121123.1:p.Arg77Gln
CA115435
NM_001127651.3:c.230G>A