Canonical Allele Identifier: PA2830359501
Gene: CYP4F22 HGNC NCBI

Linked Data

ClinVar Variation Id: 3079724
ClinVar RCV Id: RCV004370568

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775754.2:p.Arg283Gln
CA9269715
NM_173483.4:c.848G>A