Canonical Allele Identifier: PA2825212659
Gene: NCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 661353
ClinVar RCV Id: RCV000818749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000622.2:p.Gly49Arg
CA10212875
NM_000631.5:c.145G>A
CA411378865
NM_000631.5:c.145G>C