Canonical Allele Identifier: PA645466588
Gene: NCF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 294082
ClinVar RCV Id: RCV000270890
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000424.2:p.Val362Ile
CA10608452
NM_000433.4:c.1084G>A