Canonical Allele Identifier: PA2580536307
Gene: CYP4F22 HGNC NCBI

Linked Data

ClinVar Variation Id: 2324212
ClinVar RCV Id: RCV002902807
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775754.2:p.Arg284Gln
CA9269717
NM_173483.4:c.851G>A