Canonical Allele Identifier: PA645380886
Gene: CYP4F22 HGNC NCBI

Linked Data

ClinVar Variation Id: 328437
ClinVar RCV Id: RCV000323417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775754.2:p.Arg284Trp
CA9269716
NM_173483.4:c.850C>T