Canonical Allele Identifier: PA645466597
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_000424.2:p.Pro454Ser
CA1284603
NM_000433.4:c.1360C>T