Canonical Allele Identifier: PA2825648786
Gene: NCF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 947988
ClinVar RCV Id: RCV001219158
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121123.1:p.Met53Val
CA33992941
NM_001127651.3:c.157A>G