Canonical Allele Identifier: PA2825169981
Gene: NCF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 638967
ClinVar RCV Id: RCV000791651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000424.2:p.Ile7Met
CA33993122
NM_000433.4:c.21C>G