Canonical Allele Identifier: PA104982
Gene: CYP4F22 HGNC NCBI

Linked Data

ClinVar Variation Id: 911
ClinVar RCV Id: RCV000000959 RCV001731266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775754.2:p.Arg243His
CA114618
NM_173483.4:c.728G>A