Canonical Allele Identifier: PA2826164723
Gene: NCF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 294076
ClinVar RCV Id: RCV000551931 RCV000598123 RCV001668644 RCV003910066
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177723.1:p.Pro409Ser
CA1284603
NM_001190794.2:c.1225C>T