Canonical Allele Identifier: PA1139727845
Gene: NCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 953788
ClinVar RCV Id: RCV001226130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_038202.2:p.Ala83Asp
CA411379403
NM_013416.4:c.248C>A