Canonical Allele Identifier: PA645385790
Gene: NCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 341546
ClinVar RCV Id: RCV001233497
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_038202.2:p.Glu10Lys
CA10212796
NM_013416.4:c.28G>A