Canonical Allele Identifier: PA2826164429
Gene: NCF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 294076
ClinVar RCV Id: RCV000551931 RCV000598123 RCV001668644 RCV003910066
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177718.1:p.Pro373Ser
CA1284603
NM_001190789.2:c.1117C>T