Canonical Allele Identifier: PA1139679824
Gene: NCF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 946961
ClinVar RCV Id: RCV001217928
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121123.1:p.His389Asn
CA1284670
NM_001127651.3:c.1165C>A