Canonical Allele Identifier: PA2742022405
Gene: CYP4F22 HGNC NCBI

Linked Data

ClinVar Variation Id: 2748843
ClinVar RCV Id: RCV003566182
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775754.2:p.Arg187Trp
CA9269632
NM_173483.4:c.559C>T