Canonical Allele Identifier: PA2825648755
Gene: NCF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2702941
ClinVar RCV Id: RCV003498798
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121123.1:p.Met1Thr