Canonical Allele Identifier: PA2826164416
Gene: NCF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 281211
ClinVar RCV Id: RCV000309636 RCV000539456 RCV001258235 RCV001705405
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177718.1:p.Asn338Ile
CA1284632
NM_001190789.2:c.1013A>T