Canonical Allele Identifier: PA2580536291
Gene: CYP4F22 HGNC NCBI

Linked Data

ClinVar Variation Id: 2228919
ClinVar RCV Id: RCV002692355
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775754.2:p.Gln244Arg
CA9269687
NM_173483.4:c.731A>G